Updated on 2022/08/23

写真a

 
UYANIK Muhammet
 
Organization
Graduate School of Engineering Molecular and Macromolecular Chemistry 1 Associate professor
Graduate School
Graduate School of Engineering
Undergraduate School
School of Engineering Chemistry and Biotechnology
Title
Associate professor

Degree 1

  1. Doctor of Engineering ( 2007.3   Nagoya University ) 

Research Interests 4

  1. Oxidations

  2. Asymmetric Synthesis

  3. Development of Environmentally Benign Organic Reactions

  4. Oxidations

Research Areas 1

  1. Nanotechnology/Materials / Synthetic organic chemistry

Current Research Project and SDGs 1

  1. Environmentally Friendly Oxidative Transformation Reactions

Research History 2

  1. Nagoya University   Graduate School of Engineering Molecular and Macromolecular Chemistry   Associate professor

    2020.5

  2. Nagoya University   Graduate School of Engineering   Assistant Professor

    2007.4 - 2020.4

Education 3

  1. Nagoya University   Graduate School, Division of Engineering   Applied Chemistry, Chemical Engineering and Biotechnology

    2006.4 - 2007.3

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    Country: Japan

  2. Nagoya University   Graduate School, Division of Engineering   Applied Chemistry, Chemical Engineering and Biotechnology

    2004.4 - 2006.3

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    Country: Japan

  3. Nagoya University   Faculty of Engineering   Chemical and Biological Engineering

    2000.4 - 2004.3

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    Country: Japan

Professional Memberships 5

  1. The Chemical Society of Japan

  2. American Chemical Society

  3. The Society of Synthetic Organic Chemistry

  4. American Association for the Advancement of Science (AAAS)

  5. The Society of Iodine Science

Committee Memberships 3

  1. Anatolian Conference on Synthetic Organic Chemistry (ACSOC II)   Scientific Committee  

    2015.9 - 2016.3   

  2. 有機合成化学協会誌   編集協力委員  

    2014.4 - 2016.4   

  3. Turkish Journal of Chemistry (The Scientific and Technological Research Council of Turkey)   Editorial Board  

    2013.1 - 2016.12   

Awards 17

  1. Asian Core Program / Advanced Research Network Lectureship Award

    2022.7   15th International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOCA-15)   Enantioselective Ammonium Hypoiodite Catalysis for Oxidative Umpolung of Indoles

    UYANIK Muhammet

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    Award type:Award from international society, conference, symposium, etc.  Country:Hong Kong

  2. The Chemical Society of Japan Award for Young Chemists

    2017.3   The Chemical Society of Japan   Development of Selective Oxidation Reactions Using Designer Iodine Catalysts

    UYANIK Muhammet

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    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  3. Thieme Chemistry Journals Award

    2016.1   Thieme Publishing Group  

    UYANIK Muhammet

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    Award type:Award from publisher, newspaper, foundation, etc.  Country:Germany

  4. Banyu Chemist Award (BCA)

    2015.10   Banyu Life Science Foundation International   Development of Iodine Oxidation Catalysis

    UYANIK Muhammet

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    Award type:Award from publisher, newspaper, foundation, etc.  Country:Japan

  5. The 4th Green&Sustainable Chemistry (GSC) Incentive Prize

    2015.7   The Japan Association for Chemical Innovation (JACI)   Development of Environmentally Benign Catalytic Oxidation Reactions Using Iodine Compounds

    UYANIK Muhammet

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    Award type:Award from publisher, newspaper, foundation, etc.  Country:Japan

  6. 7th Inoue Science Research Award

    2015.2   Inoue Foundation for Science   Development of Enantioselective Oxidative Polyene Cyclization

    UYANIK Muhammet

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    Award type:Award from publisher, newspaper, foundation, etc.  Country:Japan

  7. The Commendation for Science and Technology by the Minister of Education, Culture, Sports, Science and Technology, The Young Scientists' Prize

    2013.4   Ministry of Education, Culture, Sports, Science and Technology, Japan   Development of Oxidation Reactions Using Designer Iodine Catalysis

    UYANIK Muhammet

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    Country:Japan

  8. The 15th SIS Symposium Poster Award

    2012.9   The Society of Iodine Science (SIS)   IBS–Catalyzed Selective Oxidation of Phenols to 1,2-Quinones with Oxone

    UYANIK Muhammet, MUTSUGA Tatsuya, ISHIHARA Kazuaki

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    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  9. The Young Scholar Lectureship Award of the CSJ

    2012.3   The Chemical Society of Japan   Environmentally benign selective oxidation reactions using hypervalent iodine catalysts

    UYANIK Muhammet

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    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  10. The Grand Prize of 6th Wakashachi Incentive Award

    2012.2   Aichi Prefectural Government  

    UYANIK Muhammet

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    Country:Japan

  11. Akazaki Prize

    2011.3   Nagoya University  

    UYANIK Muhammet

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    Country:Japan

  12. 2010 Incentive Award for Young Scientist, Tokai Branch of The Society of Synthetic Organic Chemistry

    2010.5   The Society of Synthetic Organic Chemistry, Japan  

    UYANIK Muhammet

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    Award type:Award from publisher, newspaper, foundation, etc.  Country:Japan

  13. 89th Annual Meeting of The Chemical Society of Japan, Best Presentation Award (Academic)

    2009.4   The Chemical Society of Japan  

    UYANIK Muhammet

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    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  14. Shionogi Award in Synthetic Organic Chemistry (Japan)

    2009.2   The Society of Synthetic Organic Chemistry, Japan  

    UYANIK Muhammet

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    Award type:Award from publisher, newspaper, foundation, etc.  Country:Japan

  15. 88th Annual Meeting of The Chemical Society of Japan, Best Presentation Award (Academic)

    2008.4   The Chemical Society of Japan  

    UYANIK Muhammet

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    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  16. The 4th Green & Sustainable Chemistry (GSC) Poster Award

    2008.3   Green & Sustainable Chemistry Network, Japan  

    UYANIK Muhammet

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    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  17. Bronz Medal

    1998.7   国際生物学オリンピック  

    UYANIK Muhammet

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    Award type:Award from international society, conference, symposium, etc.  Country:Germany

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Papers 54

  1. Chiral Ammonium Hypoiodite Catalysis for Enantioselective Oxidative Dearomatization Reactions Invited

    Muhammet Uyanik, Kazuaki Ishihara

      Vol. 51 ( 8 ) page: 31 - 39   2022.8

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    Authorship:Lead author, Corresponding author   Language:Japanese   Publishing type:Research paper (scientific journal)  

  2. Hypoiodite-Catalyzed Oxidative Umpolung of Indoles for Enantioselective Dearomatization Reviewed

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    Journal of the American Chemical Society   Vol. 144 ( 13 ) page: 5756 - 5761   2022.4

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    Authorship:Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/jacs.2c01852

    DOI: 10.1021/jacs.2c01852

    Web of Science

    Scopus

    Other Link: https://pubs.acs.org/doi/10.1021/jacs.2c01852

  3. Hypoiodite-catalysed oxidative homocoupling of arenols and tandem oxidation/cross-coupling of hydroquinones with arenes Reviewed

    Muhammet Uyanik, Dai Nagata, Kazuaki Ishihara

    Chemical Communications   Vol. 57 ( 88 ) page: 11625 - 11628   2021.10

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/D1CC05171G

    DOI: 10.1039/D1CC05171G

  4. Oxidative Ritter-type Chloroamidation of Alkenes Using NaCl and Oxone Invited Reviewed

    Takehiro Kato, Yuya Okada, Yuto Fujii, Muhammet Uyanik, Kazuaki Ishihara

    Asian Journal of Organic Chemistry   Vol. 10 ( 11 ) page: 2907 - 2910   2021.9

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    Authorship:Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    A practical and environmentally benign method for the oxidative Ritter-type chloroamidation of alkenes was developed using sodium chloride and oxone as a chlorinating source and an oxidant, respectively. The reaction proceeded smoothly under non-aqueous conditions without the use of any catalyst. Excellent chemoselectivity (i. e., chloroamidation versus dichlorination) could be achieved for electron-deficient styrenes. In addition, this protocol could be easily applied to 7-gram-scale synthesis.

    DOI: 10.1002/ajoc.202100575

  5. Chiral Organoiodine-catalyzed Enantioselective Oxidative Dearomatization of Phenols Invited Reviewed

    Muhammet Uyanik, Shinichi Ishizaki, Kazuaki Ishihara

    Organic Syntheses   Vol. 98   page: 28 - 50   2021.2

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.15227/orgsyn.098.0028

    Web of Science

  6. Synthesis of Chiral Organoiodine Catalyst for Enantioselective Oxidative Dearomatization Reactions: N,N'-(2S,2' S)-(2-Iodo-1,3-phenylene)bis(oxy)bis(propane-2,1-diyl)bis(2,4,6-trimethylbenzamide) Invited Reviewed

    Muhammet Uyanik, Shinichi Ishizaki, Kazuaki Ishihara

    Organic Syntheses   Vol. 98   page: 1 - 27   2021.2

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.15227/orgsyn.098.0001

    Web of Science

  7. High-Performance Hypoiodite/Hydrogen Peroxide Catalysis for Oxidative α-Azidation of Carbonyls

    Muhammet Uyanik, Naoto Sahara, Mayuko Tsukahara, Yuhei Hattori, Kazuaki Ishihara

    SIS Report   Vol. 23   page: 10 - 13   2020.12

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

  8. I+/TBHP Catalysis For Tandem Oxidative Cyclization To Indolo[2,3-b]quinolines Invited Reviewed

    Muhammet Uyanik, Hiroki Tanaka, Kazuaki Ishihara

    Asian Journal of Organic Chemistry   Vol. 10 ( 1 ) page: 164 - 169   2020.11

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    A chemoselective I+/TBHP catalysis was developed for tandem oxidative cyclization/aromatization of indole derivatives under nearly neutral conditions to give the corresponding indolo[2,3-b]quinoline sulfonate salts, which could be easily isolated via only simple filtration of the crude reaction mixture. Interestingly both ionic and radical active species would be generated in situ for the corresponding oxidative transformations to proceed in a chemoselective manner.

    DOI: 10.1002/ajoc.202000570

  9. Hypoiodite-Catalyzed Chemoselective Tandem Oxidation of Homotryptamines to Peroxy- and Epoxytetrahydropyridoindolenines Reviewed

    Muhammet Uyanik, Hiroki Tanaka, Kazuaki Ishihara

    Organic Letters   Vol. 22 ( 20 ) page: 8049 - 8054   2020.9

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    We developed the hypoiodite-catalyzed tandem dearomative peroxycyclization of homotryptamine derivatives to peroxytetrahydropyridoindolenines under mild conditions. During the course of a mechanistic study, we found that a tandem oxidative cyclization/epoxidation as an unexpected reaction proceeded in the presence of TEMPO as an additive. Intramolecular oxidative aminocyclization of homotryptamines at the C-2 position would give tetrahydropyridoindole, a common intermediate for both reactions. Control experiments suggested that while oxidative coupling with TBHP at the C-3 position might afford peroxyindolenines, a preferential electrophilic addition of TEMPO+, which might be generated in situ by the hypoiodite-catalyzed oxidation of TEMPO, at C-3 position followed by elimination and epoxidation might give epoxyindolenines. This serendipitous finding prompted us to develop a chemoselective divergent synthesis of peroxy- and epoxyindolenines by simple modification of the reaction conditions.

    DOI: 10.1021/acs.orglett.0c03001

  10. Chemo‐ and Enantioselective Oxidative α-Azidation of Carbonyl Compounds Reviewed

    Muhammet Uyanik, Naoto Sahara, Mayuko Tsukahara, Yuhei Hattori, Kazuaki Ishihara

    Angewandte Chemie International Edition   Vol. 59 ( 39 ) page: 17110 - 17117   2020.6

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    We report high-performance I+/H2O2 catalysis for the oxidative or decarboxylative oxidative α-azidation of carbonyl compounds by using sodium azide under biphasic neutral phase-transfer conditions. To induce higher reactivity especially for the α-azidation of 1,3-dicarbonyl compounds, we designed a structurally compact isoindoline-derived quaternary ammonium iodide catalyst bearing electron-withdrawing groups. The nonproductive decomposition pathways of I+/H2O2 catalysis could be suppressed by the use of a catalytic amount of a radical-trapping agent. This oxidative coupling tolerates a variety of functional groups and could be readily applied to the late-stage α-azidation of structurally diverse complex molecules. Moreover, we achieved the enantioselective α-azidation of 1,3-dicarbonyl compounds as the first successful example of enantioselective intermolecular oxidative coupling with a chiral hypoiodite catalyst.

    DOI: 10.1002/anie.202007552

  11. Chemoselective oxidative generation of ortho-quinone methides and tandem transformations Reviewed

    Muhammet Uyanik, Kohei Nishioka, Ryutaro Kondo, Kazuaki Ishihara

    Nature Chemistry   Vol. 12 ( 4 ) page: 353 - 362   2020.3

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    ortho-Quinone methides are useful transient synthetic intermediates in organic synthesis. These species are most often generated in situ by the acid- or base-mediated transformation of phenols that have been pre-functionalized at a benzylic position, or by biomimetic oxidation of the corresponding ortho-alkylphenols with metal oxidants or transition-metal complexes. Here we describe a method for the transition-metal-free oxidative generation of o-QMs from ortho-alkylarenols, using hypoiodite catalysis under nearly neutral conditions, which can then be applied in one-pot tandem reactions. This method for the chemoselective oxidative generation of ortho-quinone methides may prove superior to previous methods with respect to environmental issues and scope, and can be applied to various tandem reactions such as inter- or intramolecular [4 + 2] cycloaddition, oxa-6π-electrocyclization, conjugate addition and spiroepoxidation.

    DOI: 10.1038/s41557-020-0433-4

  12. Chemoselective Oxidative Spiroetherification and Spiroamination of Arenols Using I+/Oxone Catalysis Reviewed

    Muhammet Uyanik, Naoto Sahara, Outa Katade, Kazuaki Ishihara

    Organic Letters   Vol. 22 ( 2 ) page: 560 - 564   2019.12

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    We developed a chemoselective oxidative dearomative spiroetherification and spiroamination of arenols using I+/oxone catalysis. The intramolecular dearomative C–O and C–N couplings proceeded much more efficiently under slightly acidic conditions to give the corresponding spiro adducts in higher yields compared with previous methods using transition metal or hypervalent iodine catalysts. Control experiments suggested that both hypoiodous acid and iodine might be active species for these reactions.

    DOI: 10.1021/acs.orglett.9b04324

  13. Designer C2-symmetric Chiral Diamide-type Organoiodine Catalysts Invited

    Muhammet Uyanik, Kazuaki Ishihara

    TCI Mail   Vol. 2019 ( 182 ) page: 2 - 16   2019.12

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    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)  

    As the global issues of environment, energy, and natural resource scarcity increase, the development
    of environmentally friendly and efficient catalytic methodologies of organic synthesis is strongly demanded for the sustainable advancement of material civilization. For this purpose, the use of toxic heavy metals and precious transition metals as reactants and/or catalysts should be avoided as much as possible in the synthesis of medicinal and pharmaceutical products. Over the past decades, iodine compounds have been the focus of great attention due to their mild and chemoselective oxidizing properties and their environmentally benign characteristics in contrast to
    toxic metal oxidants. Furthermore, the development of chiral hypervalent iodine-catalyzed enantioselective oxidative transformation is one of the most challenging areas in asymmetric organocatalysis. Here, we demonstrate the rational
    design of conformationally flexible chiral diamide-type C2-symmetric organoiodine catalysis based on secondary
    nonbonding interactions for the enantioselective oxidative dearomatization of arenols. Several research groups
    have also reported highly enantioselective oxidative transformations using these conformationally flexible chiral
    organoiodine(III) catalysts or reagents. These examples highlight the substantial scope of conformationally flexible designer organoiodine(III) catalysis.

  14. デザイナーC2-対称ジアミド型キラルヨードアレーン触媒 Invited

    ウヤヌク ムハメット, 石原一彰

    TCIメール   Vol. 2019 ( 182 ) page: 2 - 16   2019.12

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    Authorship:Corresponding author   Language:Japanese   Publishing type:Research paper (scientific journal)  

    環境・エネルギー・資源問題が深刻化するなか,物質文明社会の持続的発展のためには,環境低負荷型触媒的精密有機合成法の開拓が有機合成化学の最重要課題の一つであり,遷移金属等のレアメタルや重金属等の毒性の強い金属資源を反応剤や触媒に用いる従来型の有機合成化学からの脱却が求められている。これに関連し近年,有毒な重金属酸化物の代替物質として超原子価ヨウ素化合物が注目されている。しかし,超原子価ヨウ素の化学は1世紀以上の長い歴史をもつにもかかわらず,不斉酸化反応の成功例はほとんどなく,不斉有機触媒の最も挑戦的な課題の一つとされていた。我々は,それまでの触媒設計概念とは全く異なる配座柔軟性に富むキラルヨードアレーンを分子設計した。本設計は,触媒活性中心(I(III))と側鎖末端の間に適切な非共有結合性二次的相互作用を導入することで有効な不斉場を構築することを特徴とし,酵素反応に見られる誘導適合のような不斉誘導が可能となる。これらの柔軟かつ機能的な触媒は,様々な酸化的変換反応において世界中で利用されるようになってきている。本総説では我々のC 2対称ジアミド型触媒設計とその応用例について紹介する。

  15. High-Performance Ammonium Hypoiodite/Oxone Catalysis for Enantioselective Oxidative Dearomatization of Arenols Reviewed

    Muhammet Uyanik, Takehiro Kato, Naoto Sahara, Outa Katade, Kazuaki Ishihara

    ACS Catalysis   Vol. 9 ( 12 ) page: 11619 - 11626   2019.11

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    A high-performance enantioselective quaternary ammonium hypoiodite catalysis was developed for the dearomatization of arenols using oxone as an environmentally benign oxidant. The oxidation of not only 1- and 2-naphthols but also phenols, which were hardly reactive using the previous hypoiodite catalysis, readily proceeded under mild conditions, and only inorganic wastes were generated from the oxidant used. Control experiments and Raman analysis revealed the in situ generation of I+ such as hypoiodous acid as an unstable active species and molecular iodine (I2) as a stable dormant species. Most of the advantages of the present I+/oxone catalysis, compared to previous I+/(H2O2 or ROOH) systems, may result from generation of the stable dormant state and the higher reactivity of catalysts under acidic conditions.

    DOI: 10.1021/acscatal.9b04322

  16. Ammonium Hypoiodite-Catalyzed Oxidative Dearomatizative Azidation of Arenols Reviewed

    Muhammet Uyanik, Kohei Nishioka, Kazuaki Ishihara

    Chemistry Letters   Vol. 48 ( 4 ) page: 353 - 356   2019.1

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    The first transition metal-free catalytic oxidative dearomatizative azidation of arenols has been developed using hypoiodite catalysis with aqueous hydrogen peroxide and trimethylsilyl azide as an oxidant and azide source, respectively, under mild conditions. The corresponding quaternary azides can be obtained in high to excellent yields.

    DOI: 10.1246/cl.181036

  17. Front Cover: Regioselective Oxidative Chlorination of Arenols Using NaCl and Oxone (Eur. J. Org. Chem. 1/2019) Reviewed

    Muhammet Uyanik, Naoto Sahara, Kazuaki Ishihara

    European Journal of Organic Chemistry   Vol. 2019 ( 1 ) page: 1 - 1   2019.1

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    DOI: 10.1002/ejoc.201801769

  18. Regioselective Oxidative Chlorination of Arenols Using NaCl and Oxone Invited Reviewed

    Muhammet Uyanik, Naoto Sahara, Kazuaki Ishihara

    European Journal of Organic Chemistry   Vol. 2019 ( 1 ) page: 27 - 31   2018.10

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    We developed a practical and environmentally benign method for the chlorinative dearomatization of arenols using transient electrophilic chlorinating species generated in situ from inexpensive sodium chloride and Oxone as a Cl source and oxidant, respectively, under mild conditions. Moreover, the regioselective chlorination or chlorinative dearomatization of 1-naphthols was also achieved by changing the reaction conditions.

    DOI: 10.1002/ejoc.201801063

  19. Asymmetric Total Synthesis of (-)-Maldoxin, a Common Biosynthetic Ancestor of the Chloropupukeananin Family Reviewed

    Takahiro Suzuki, Soichiro Watanabe, Muhammet Uyanik, Kazuaki Ishihara, Susumu Kobayashi, Keiji Tanino

    Organic Letters   Vol. 20 ( 20 ) page: 3919 - 3922   2018.6

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    The total synthesis of pestheic acid based on an intramolecular SNAr reaction without a nitro group and the asymmetric synthesis of (-)-maldoxin by a catalytic enantioselective oxidative dearomatization of pestheic acid are described. The reactivity of (-)-maldoxin as a diene in the Diels-Alder reaction is also investigated.

    DOI: 10.1021/acs.orglett.8b01502

  20. Chiral Hypervalent Organoiodine-Catalyzed Enantioselective Oxidative Spirolactonization of Naphthol Derivatives Reviewed

    Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

    The Journal of Organic Chemistry   Vol. 82 ( 22 ) page: 11946 - 11953   2017.9

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    Highly enantioselective oxidative dearomatization of 2-naphthol derivatives was achieved for the first time by using conformationally flexible organoiodine catalysts derived from 2-aminoalcohol as a chiral source. Moreover, with the use of these catalysts, excellent enantioselectivities were also achieved for 1-naphthol derivatives, which had previously been obtained with only lower enantioselectivities. Furthermore, the product obtained from the present reaction could be transformed to a highly functionalized spirolactone in high yield and with excellent stereoselectivity.

    DOI: 10.1021/acs.joc.7b01941

  21. 4,5-Dimethyl-2-Iodoxybenzenesulfonic Acid Catalyzed Site-Selective Oxidation of 2-Substituted Phenols to 1,2-Quinols Reviewed

    Muhammet Uyanik, Tatsuya Mutsuga, Kazuaki Ishihara

    Angewandte Chemie International Edition   Vol. 56 ( 14 ) page: 3956 - 3960   2017.2

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    A site-selective hydroxylative dearomatization of 2-substituted phenols to either 1,2-benzoquinols or their cyclodimers, catalyzed by 4,5-dimethyl-2-iodoxybenzenesulfonic acid with Oxone, has been developed. Furthermore, both the reaction rate and site selectivity could be further improved by the introduction of a trialkylsilylmethyl substituent at the 2-position of phenols. The corresponding 1,2-quinols could be transformed into various useful structural motifs by [4+2] cycloaddition cascade reactions.

    DOI: 10.1002/anie.201612463

  22. Ammonium Hypoiodite-Catalyzed Peroxidative Dearomatization of Phenols Invited Reviewed

    Muhammet Uyanik, Kohei Nishioka, Kazuaki Ishihara

    Heterocycles   Vol. 95 ( 2 ) page: 1132 - 1147   2017.1

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    Here, we report the first transition metal-free peroxidative dearomatization of phenols using hypoiodite catalysis with TBHP. Hypoiodite salts are generated in situ from the corresponding quaternary ammonium iodides in the presence of TBHP, and the oxidative coupling reaction proceeds efficiently under mild conditions. The dearomatized products are versatile synthetic intermediates for further synthetic transformations to various complex structures including heterocycles. As a demonstration, the further oxidation of the unsaturated peroxide with TBHP afforded the corresponding peroxy epoxide in good yield.

    DOI: 10.3987/COM-16-S(S)84

  23. Enantioselective Synthesis of Masked Benzoquinones Using Designer Chiral Hypervalent Organoiodine(III) Catalysis Reviewed

    Muhammet Uyanik, Niiha Sasakura, Masahiro Mizuno, Kazuaki Ishihara

    ACS Catalysis   Vol. 7 ( 1 ) page: 872 - 876   2016.12

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)  

    A highly enantioselective oxidative dearomatization of ortho- and para-hydroquinone derivatives to the corresponding masked ortho- and para-benzoquinones has been achieved by using chiral organoiodine(III) catalysts.

    DOI: 10.1021/acscatal.6b03380

  24. Chiral Quaternary Ammonium Hypoiodite Catalysis Invited

      Vol. 45 ( 12 ) page: 16 - 24   2016.12

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    Authorship:Lead author, Corresponding author   Language:Japanese   Publishing type:Research paper (scientific journal)  

  25. Chiral Ammonium Hypoiodite Salt-Catalyzed Enantioselective Oxidative Cycloetherification to 2-Acyl Tetrahydrofurans Reviewed

    Muhammet Uyanik, Hiroki Hayashi, Hirokazu Iwata, Kazuaki Ishihara

    Chemistry Letters   Vol. 45 ( 3 ) page: 353 - 355   2016.1

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    2-Acyl tetrahydrofuran is a fundamental structure in natural products and pharmaceuticals. We achieved a chiral quaternary ammonium hypoiodite salt-catalyzed enantioselective oxidative cycloetherification of δ-hydroxyketone derivatives. The corresponding 2-acyl tetrahydrofurans were obtained in high chemical yield with high enantioselectivity.

    DOI: 10.1246/cl.160004

  26. Practical Oxidative Dearomatization of Phenols with Sodium Hypochlorite Pentahydrate Reviewed

    Muhammet Uyanik, Niiha Sasakura, Mitsuyoshi Kuwahata, Yasukazu Ejima, Kazuaki Ishihara

    Chemistry Letters   Vol. 44 ( 3 ) page: 381 - 383   2015.2

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    A highly efficient and practical oxidative dearomatization of phenols using sodium hypochlorite pentahydrate as an inexpensive, strong oxidant is reported for the first time. The oxidation reactions proceeded very rapidly in the presence of water to give the desired products in excellent yields, and sodium chloride and water were the only by-products derived from the oxidant.

    DOI: 10.1246/cl.141130

  27. High-Performance Hypoiodite/Hydrogen Peroxide Catalytic System for the Oxylactonization of Aliphatic γ-Oxocarboxylic Acids Reviewed

    Muhammet Uyanik, Daisuke Suzuki, Mizu Watanabe, Hiroyasu Tanaka, Kikuo Furukawa, Kazuaki Ishihara

    Chemistry Letters   Vol. 44 ( 3 ) page: 387 - 389   2015.2

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    Highly efficient hypoiodite-catalyzed oxylactonization of aliphatic γ-oxocarboxylic acids to the corresponding γ-acyl-γ-butyrolactones was developed. Highly dilute reaction conditions and slow addition of the oxidant are each highly effective for promoting the high-performance hypoiodite/hydrogen peroxide catalytic oxidation system.

    DOI: 10.1246/cl.141110

  28. Chiral Ammonium Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of 1-Naphthols Using Hydrogen Peroxide Reviewed

    Muhammet Uyanik, Niiha Sasakura, Erina Kaneko, Kento Ohori, Kazuaki Ishihara

    Chemistry Letters   Vol. 44 ( 2 ) page: 179 - 181   2015.2

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    A highly enantioselective oxidative dearomatization of 1-naphthol derivatives (Kita spirolactonization) catalyzed by chiral hypoiodite species prepared in situ from chiral quaternary ammonium iodide in the presence of hydrogen peroxide is reported.

    DOI: 10.1246/cl.141012

  29. High-turnover hypoiodite catalysis for asymmetric synthesis of tocopherols Reviewed

    Muhammet Uyanik, Hiroki Hayashi, Kazuaki Ishihara

    Science   Vol. 345 ( 6194 ) page: 291 - 294   2014.7

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    The diverse biological activities of tocopherols and their analogs have inspired considerable interest in the development of routes for their efficient asymmetric synthesis. Here, we report that chiral ammonium hypoiodite salts catalyze highly chemo- and enantioselective oxidative cyclization of γ-(2-hydroxyphenyl)ketones to 2-acyl chromans bearing a quaternary stereocenter, which serve as productive synthetic intermediates for tocopherols. Raman spectroscopic analysis of a solution of tetrabutylammonium iodide and tert-butyl hydroperoxide revealed the in situ generation of the hypoiodite salt as an unstable catalytic active species and triiodide salt as a stable inert species. A high-performance catalytic oxidation system (turnover number of ~200) has been achieved through reversible equilibration between hypoiodite and triiodide in the presence of potassium carbonate base. We anticipate that these findings will open further prospects for the development of high-turnover redox organocatalysis.

    DOI: 10.1126/science.1254976

  30. Selective Oxidation Reactions Using 2-Iodobenzenesulfonic Acid (pre-IBS) and Oxone Invited

    Wako Junyaku Jiho   Vol. 81 ( 4 ) page: 5 - 9   2013.10

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  31. Hydrogen Bonding and Alcohol Effects in Asymmetric Hypervalent Iodine Catalysis: Enantioselective Oxidative Dearomatization of Phenols Reviewed

    Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

    Angewandte Chemie International Edition   Vol. 52 ( 35 ) page: 9215 - 9218   2013.6

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    A conformationally flexible C2-symmetric organoiodine(III) catalyst for the highly enantioselective catalytic oxidative dearomatization of phenols has been developed. Catalysis is controlled by intramolecular hydrogen-bonding interactions and additional achiral alcohols.

    DOI: 10.1002/anie.201303559

  32. Baeyer-Villiger Oxidation Using Hydrogen Peroxide Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara

    ACS Catalysis   Vol. 3 ( 5 ) page: 513 - 520   2013.2

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    The Baeyer-Villiger (BV) oxidation of carbonyl compounds to the corresponding esters or lactones is one of the most important transformations. We recently introduced a highly efficient and selective LiB(C6F5)4- or Ca[B(C6F5)4]2-catalyzed BV oxidation of ketones with aqueous hydrogen peroxide to give the corresponding lactones in high yield. In this perspective article, we focus on our discovery and the development of BV oxidation reactions and cascade oxidative transformations through representative metal catalysts and organocatalysts.

    DOI: 10.1021/cs300821u

  33. Conformationally-Flexible Chiral Hypervalent Organoiodine Catalysts for Enantioselective Oxidative Transformations Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara

    Journal of Synthetic Organic Chemistry, Japan   Vol. 70 ( 11 ) page: 1116 - 1122   2012.11

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    The development of chiral hypervalent iodine-catalyzed oxidative transformations is one of the most challenging areas in asymmetric organocatalysis. Although several elegant chiral hypervalent iodine(III and V) reagents or catalysts had been developed for various asymmetric oxidation reactions, the enantioselectivities had been moderate before our paper was published in 2010. We have had a great interest in the development of organocatalysis based on hypervalent chemistry since 2007. In this account, we describe our design concept of conformationally-flexible chiral hypervalent organoiodine(III), and the results obtained for catalytic use of our chiral iodines(III) for enantioselective Kita oxidative spirolactonization. Additionally, other chiral hypervalent iodine-mediated asymmetric oxidation reactions reported after our publications are also highlighted briefly.

    DOI: 10.5059/yukigoseikyokaishi.70.1116

    Web of Science

  34. Baeyer-Villiger Oxidation and Oxidative Cascade Reactions with Aqueous Hydrogen Peroxide Catalyzed by Lipophilic Li[B(C6F5)4] and Ca[B(C6F5)4]2 Reviewed

    Muhammet Uyanik, Daisuke Nakashima, Kazuaki Ishihara

    Angewandte Chemie International Edition   Vol. 51 ( 36 ) page: 9093 - 9096   2012.8

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    We have developed highly efficient and selective Li[B(C6F5)4] or Ca[B(C6F5)4]2 catalyzed Baeyer-Villiger (BV) oxidations of various cycloalkanones with 30-wt% aqueous hydrogen peroxide to give the corresponding lactones in high yield. Additionally, we have found that the reaction rate is accelerated with the use of oxalic acid as a co-catalyst. Moreover, beta-silyl cyclohexanones can be oxidized to either the corresponding unsaturated carboxylic acids or hydroxylactones in high yields through BV oxidation/b-elimination reaction sequences and subsequent epoxidation/cyclization reaction sequences, by controlling the amounts of H2O2 and oxalic acid. These reactions proceed under mild conditions and tolerate various functional groups.

    DOI: 10.1002/anie.201204286

  35. Eco-friendly selective oxidation reactions using designed iodine catalysts Reviewed

    Chemistry and Chemical Industry   Vol. 65 ( 8 ) page: 625 - 626   2012.8

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  36. IBS-Catalyzed Regioselective Oxidation of Phenols to 1,2-Quinones with Oxone Invited Reviewed

    Muhammet Uyanik, Tatsuya Mutsuga, Kazuaki Ishihara

    Molecules   Vol. 17 ( 7 ) page: 8604 - 8616   2012.7

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    We have developed the first example of hypervalent iodine(V)-catalyzed regioselective oxidation of phenols to ortho-quinones. Various phenols could be oxidized to the corresponding ortho-quinones in good to excellent yields using catalytic amounts of sodium salts of 2-iodobenzenesulfonic acids (pre-IBSes) and stoichiometric amounts of Oxone as a co-oxidant under mild conditions. The reaction rate of IBS-catalyzed oxidation under nonaqueous conditions was further accelerated in the presence of an inorganic base such as potassium carbonate (K2CO3), a phase transfer catalyst such as tetrabutylammonium hydrogen sulfate (n-Bu4NHSO4), and a dehydrating agent such as anhydrous sodium sulfate (Na2SO4).

    DOI: 10.3390/molecules17078604

  37. Catalysis with In Situ-Generated (Hypo)iodite Ions for Oxidative Coupling Reactions Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara

    ChemCatChem   Vol. 4 ( 2 ) page: 177 - 185   2011.12

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    This Concept highlights the discovery and development of oxidative coupling reactions catalyzed by the hypoiodite (IO) or iodite (IO2) ion, which are generated in situ from iodide (I-) ion with hydrogen peroxide or tert-butyl hydroperoxide as an environmentally benign oxidant. The most important features of these catalytic systems are 1) metal-free oxidation, 2) milder reaction conditions, 3) high chemoselectivity (they tolerate a wide range of various functional groups), 4) operational simplicity, and 5) water or tert-butyl alcohol as the only byproduct derived from the co-oxidant used.

    DOI: 10.1002/cctc.201100352

  38. 2-Iodoxy-5-Methylbenzenesulfonic Acid-Catalyzed Selective Oxidation of 4-Bromobenzyl Alcohol to 4-Bromobenzaldehyde or 4-Bromobenzoic Acid with Oxone Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara, Margaret Faul, Richard Crockett

    Organic Syntheses   Vol. 89   page: 105 - 114   2011.9

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    We have reported that 2-iodoxybenzenesulfonic acids (IBSs) which are in situ prepared from Oxone and 2-iodobenzenesulfonic acids show efficient catalytic activity on the alcohol oxidation under mild conditions. Here, we succeeded in scale up of the IBS-catalyzed alcohol oxidations.

    DOI: 10.15227/orgsyn.089.0105

  39. In Situ Generated (Hypo)Iodite Catalysts for the Direct α-Oxyacylation of Carbonyl Compounds with Carboxylic Acids Reviewed

    Muhammet Uyanik, Daisuke Suzuki, Takeshi Yasui, Kazuaki Ishihara

    Angewandte Chemie International Edition   Vol. 50 ( 23 ) page: 5331 - 5334   2011.5

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    The intra- and intermolecular title reaction is catalyzed by an in situ generated ammonium (hypo)iodite species. Either H2O2 or tert-butyl hydroperoxide (TBHP) can be used as an environmentally benign oxidant and a wide range of substrates react to give the corresponding alpha-acyloxycarbonyl compounds in good to excellent yields.

    DOI: 10.1002/anie.201101522

  40. Design of Chiral Hypervalent Iodine Catalysts Using Nonbonding Interactions: Application to Kita Spirolactonization Invited

    Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

    Wako Junyaku Jiho   Vol. 79 ( 2 ) page: 2-5   2011.4

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  41. In Situ-Generated Chiral Quaternary Ammonium (Hypo)iodite Catalysis for Enantioselective Oxidative Cyclisations Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara

    Chimica Oggi-Chemistry Today   Vol. 29 ( 1 ) page: 18 - 21   2011.1

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    Very recently, we developed the first enantioselective oxidative cycloetherification of ketophenols to 2-acyl-2,3-dihydrobenzofuran derivatives catalysed by in situ generated chiral quaternary ammonium (hypo)iodite with hydrogen peroxide or tert-butyl hydroperoxide (TBHP) as an environmentally benign ideal oxidant. The optically active
    2-acyl 2,3-dihydrobenzofuran skeleton is a key structure in
    several medicinally and biologically active compounds.

  42. 2-Iodoxybenzenesulfonic Acid (IBS)-Catalyzed Oxidation of Alcohols Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara

    Aldrichimica Acta   Vol. 43 ( 3 ) page: 83 - 91   2010.12

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    The oxidation of alcohols to the corresponding carbonyl compounds is one of the most important transformations in synthetic organic chemistry. Over the past two decades, hypervalent iodine compounds have received a great deal of attention due to their mild and chemoselective oxidizing properties and to the fact that, unlike toxic heavy-metal-based reagents, they are environmentally benign. We recently published a review on the oxidation of alcohols with stoichiometric or catalytic hypervalent iodine compounds. The present review focuses on the discovery and development of 2-iodoxybenzenesulfonic acid (IBS) and related hypervalent iodine compounds. It also covers advances in hypervalent iodine catalyzed alcohol oxidations and related transformations reported between 2005 and 2010.

  43. Catalytic asymmetric oxidative coupling without metals. Breakthrough to inorganic iodites Invited

    Kazuaki Ishihara, Muhammet Uyanik

    Kagaku   Vol. 65 ( 10 ) page: 12 - 17   2010.9

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  44. Quaternary Ammonium (Hypo)iodite Catalysis for Enantioselective Oxidative Cycloetherification Reviewed

    Muhammet Uyanik, Hiroaki Okamoto, Takeshi Yasui, Kazuaki Ishihara

    Science   Vol. 328 ( 5984 ) page: 1376 - 1379   2010.6

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    It is desirable to minimize the use of rare or toxic metals for oxidative reactions in the synthesis of pharmaceutical products. Hypervalent iodine compounds are environmentally benign alternatives, but their catalytic use, particularly for asymmetric transformations, has been quite limited. We report here an enantioselective oxidative cycloetherification of ketophenols to 2-acyl-,3-dihydrobenzofuran derivatives, catalyzed by in situ generated chiral quaternary ammonium (hypo)iodite salts, with hydrogen peroxide as an environmentally benign oxidant. The optically active 2-acyl 2,3-dihydrobenzofuran skeleton is a key structure in several biologically active compounds.

    DOI: 10.1126/science.1188217

  45. Chiral Hypervalent Iodine-Catalyzed Enantioselective Oxidative Kita Spirolactonization of 1-Naphthol Derivatives and One-Pot Diastereoselective Oxidation to Epoxyspirolactones Invited Reviewed

    Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

    Tetrahedron   Vol. 66 ( 31 ) page: 5841 - 5851   2010.4

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    We demonstrate here the rational design of a conformationally flexible C2-symmetric iodosylarene 8g based on secondary n-sigma* or hydrogen-bonding interactions as a chiral catalyst for the enantioselective Kita oxidative spirolactonization of 1-naphthol derivatives 5. Iodosylarenes 8 were generated in situ from iodoarenes 7 and mCPBA as a co-oxidant. Furthermore, epoxyspirolactone 15 was obtained by the one-pot oxidation of 5 with mCBPA in the presence of 7g. Thus, the enantioselective oxidation of 5 to 6 and the successive enantio- and diastereo-selective oxidation of 5 to 15 proceeded in good yields when we controlled the amount of mCPBA.

    DOI: 10.1016/j.tet.2010.04.060

  46. Enantioselective Kita Oxidative Spirolactonization Catalyzed by In Situ Generated Chiral Hypervalent Iodine(III) Species Reviewed

    Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

    Angewandte Chemie International Edition   Vol. 49 ( 12 ) page: 2175 - 2177   2010.3

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    Conformationally flexible C2-symmetric chiral iodosylarene, which has been rationally designed based on secondary n-σ* or hydrogen-bonding interactions, is a highly effective catalyst for the Kita oxidative spirolactonization. The present catalysis is applicable to a broader range of substrates and provides the highest enantioselectivity (up to 92% ee) among previous chiral hypervalent iodine-catalyzed reactions.

    DOI: 10.1002/anie.200907352

  47. Bromine-Catalyzed Aerobic Oxidation of Alcohols Invited Reviewed

    Muhammet Uyanik, Ryota Fukatsu, Kazuaki Ishihara

    Chemistry-An Asian Journal   Vol. 5 ( 3 ) page: 456 - 460   2010.2

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    We demonstrated that a simple and environmentally benign catalytic system HBr/NaNO2 is very effective for the selective oxidation of alcohols under balloon pressure of O2. Furthermore, the aerobic oxidation of alcohols was also achieved under balloon pressure of air instead of pure O2 with this HBr/NaNO2/HNO3 catalytic system.

    DOI: 10.1002/asia.200900609

  48. IBS-Catalyzed Oxidative Rearrangement of Tertiary Allylic Alcohols to Enones with Oxone Reviewed

    Muhammet Uyanik, Ryota Fukatsu, Kazuaki Ishihara

    Organic Letters   Vol. 11 ( 15 ) page: 3470 - 3473   2009.7

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    A 2-iodoxybenzenesulfonic acid (IBS)-catalyzed oxidative rearrangement of tertiary allylic alcohols to enones with powdered Oxone in the presence of potassium carbonate and tetrabutylammonium hydrogen sulfate has been developed.

    DOI: 10.1021/ol9013188

  49. Hypervalent iodine-catalyzed oxylactonization of ketocarboxylic acids to ketolactones Invited Reviewed

    Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

    Bioorganic & Medicinal Chemistry Letters   Vol. 19 ( 14 ) page: 3848 - 3851   2009.4

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    The hypervalent iodine-catalyzed oxylactonization of ketocarboxylic acids to ketolactones was achieved in the presence of iodobenzene (10 mol%), p-toluenesulfonic acid monohydrate (20 mol%) and meta-chloroperbenzoic acid as a stoichiometric co-oxidant.

    DOI: 10.1016/j.bmcl.2009.03.148

  50. Hypervalent Iodine-Mediated Oxidation of Alcohols Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara

    Chemical Communications   Vol. 2009 ( 16 ) page: 2086 - 2099   2009.3

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    Over the past two decades there has been a dramatic increse in the use of hypervalent iodine compounds in synthetic organic chemistry due to their mild and selective oxidizing properties. Hypervalent iodine compounds catalyze various oxidation reactions such as the oxidation of alcohols, alpha-oxidation of ketones, oxidative spirocyclization of phenols, etc. Very recently, we found that 2-iodoxybenzensulfonic acid (IBS), which was generated from 2-iodobenzenesulfonic acid in situ, was an extremely active and mild catalyst for the highly chemoselective oxidation of various alcohols with powdered Oxone to carbonyl compounds such as aldehydes, carboxylic acids, ketones and cycloalkenones under nonaqueous conditions. In this review, we focus on the design of hypervalent iodine catalysts and review the discovery and development of the oxidation of alcohols with the stoichiometric or catalytic use of hypervalent iodine compounds.

    DOI: 10.1039/b823399c

  51. 2-Iodoxybenzenesulfonic Acid as an Extremely Active Catalyst for the Selective Oxidation of Alcohols to Aldehydes, Ketones, Carboxylic Acids, and Enones with Oxone Reviewed

    Muhammet Uyanik, Matsujiro Akakura, Kazuaki Ishihara

    Journal of the American Chemical Society   Vol. 131 ( 1 ) page: 251 - 262   2008.12

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    Electron-donating group-substituted 2-iodoxybenzoic acids (IBXs) were superior to IBX as catalysts for the oxidation of alcohols with Oxone under nonaqueous conditions. Furthermore, 2-iodoxybenzenesulfonic acid (IBS) was much more active than modified IBXs. Thus, we established a highly efficient and selective method for the oxidation of primary and secondary alcohols to carbonyl compounds such as aldehydes, carboxylic acids, and ketones with Oxone in nonaqueous nitromethane, acetonitrile, or ethyl acetate in the presence of 0.05-5 mol % of IBS, which was generated in situ from 2-iodobenzenesulfonic acid or its sodium salt. Cycloalkanones could be further oxidized to α,β-cycloalkenones or lactones by controlling the amounts of Oxone under the same conditions as above. Based on theoretical calculations, we considered that the relatively ionic character of the intramolecular hypervalent iodine-OSO2 bond of IBS might lower the twisting barrier of the alkoxyperiodinane intermediate.

    DOI: 10.1021/ja807110n

  52. Catalytic Diastereoselective Polycyclization of Homo(polyprenyl)arene Analogues Bearing Terminal Siloxyvinyl Groups Reviewed

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    Organic Letters   Vol. 8 ( 24 ) page: 5649 - 5652   2006.11

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    Highly diastereoselective polycyclization of homo(polyprenyl)arene analogues bearing terminal siloxyvinyl groups was catalyzed by tin(IV) chloride (10 mol %). The cyclizations of tert-butyldiphenylsilyl and triisopropylsilyl polyenol ethers gave 4(equatorial)- and 4(axial)-siloxypolycycles as major isomers, respectively. The strong nucleophilicity of pro-C(9), a (6E) geometry, and a bulky silyl group effectively favored the 4-preference, whereas the weak nucleophilicity of pro-C(9), a (6Z)-geometry, and less steric hindrance of a silyl group favored the 4-preference.

    DOI: 10.1021/ol062378t

  53. Biomimetic Synthesis of Acid-Sensitive (-)- and (+)-Caparrapi Oxides, (-)- and (+)-8-Epicaparrapi Oxides, and (+)-Dysifragin Induced by Artificial Cyclases Invited Reviewed

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    Bioorg. Med. Chem.   Vol. 13 ( 17 ) page: 5055 - 5065   2005.5

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    Asymmetric total syntheses of acid-sensitive (-)- and (+)-caparrapi oxides (1) and (+)-8-epicaparrapi oxide (2) from farnesol (10) are achieved using Sharpless-Katsuki epoxidation and Lewis acid-assisted chiral Br?nsted acid (chiral LBA)-induced polyene cyclization as key steps. The relative configuration of (+)-dysifragin (4) is determined by a single-crystal X-ray diffraction and its total synthesis is accomplished by the diastereoselective epoxidation of (+)-1. Furthermore, (-)-1 can be directly synthesized from (S)-nerolidol (3) and (R)-LBA with 88% ds by reagent control, which overcame substrate control, while (-)-2 is obtained from (R)-3 and (R)-LBA with >99% ds by the double asymmetric induction.

    DOI: 10.1016/j.bmc.2005.04.029

  54. Biomimetic Synthesis of Acid-Sensitive (-)-Caparrapi Oxide and (+)-8-Epicaparrapi Oxide Induced by Artificial Cyclases Reviewed

    Muhammet Uyanik, Hideaki Ishibashi, Kazuaki Ishihara, Hisashi Yamamoto

    Organic Letters   Vol. 7 ( 8 ) page: 1601 - 1604   2005.3

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    Asymmetric total syntheses of acid-sensitive (-)-caparrapi oxide (1) and (+)-8-epicaparrapi oxide (2) from farnesol (9) were achieved using Sharpless-Katsuki epoxidation and Lewis acid-assisted chiral Brnsted acid (chiral LBA)-induced polyene cyclization as key steps. Furthermore, (-)-1 could be directly synthesized from (S)-nerolidol (3) and (R)-LBA with 88% ds by reagent control which overcame substrate control, while (-)-2 was obtained from (R)-3 and (R)-LBA with >99% ds by the double-asymmetric induction.

    DOI: 10.1021/o1050295r

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Books 8

  1. Asymmetric Hypervalent Iodine Catalysis, In: Catalytic Asymmetric Synthesis, 4th Ed., Takahiko Akiayama and Iwao Ojima (Eds.) Reviewed

    Muhammet Uyanik, Kazuaki Ishihara( Role: Sole author ,  Chapter 7)

    John Wiley & Sons: Hooboken  2022.6  ( ISBN:9781119736424

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    Responsible for pages:pp. 243-276   Language:English Book type:Scholarly book

    DOI: 10.1002/9781119736424.ch7

    Other Link: https://onlinelibrary.wiley.com/doi/10.1002/9781119736424.ch7

  2. Catalytic Oxidative alpha-Functionalization of Carbonyls, In: Iodine Catalysis in Organic Synthesis, Kazuaki Ishihara and Kilian Muñiz (Eds.) Reviewed

    Muhammet Uyanik( Role: Sole author ,  Chapter 10)

    Wiley-VCH: Weinheim  2022.1  ( ISBN:9783527348299

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  3. Oxidation of Alcohols and Amines, In: Patai's Chemistry of Functional Groups, Ilan Marek, Berit Olofsson and Zvi Rappoport (Eds.) Reviewed

    Muhammet Uyanik, Kazuaki Ishihara( Role: Joint author)

    John Wiley & Sons: Chichester  2019.4  ( ISBN:9781119352303

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    Total pages:1032   Responsible for pages:pp. 261-306   Language:English Book type:Scholarly book

    DOI: 10.1002/9780470682531.pat0945

    Other Link: https://www.amazon.com/Chemistry-Hypervalent-Halogen-Compounds-Functional/dp/1119352304

  4. alpha-Oxidation of Carbonyl Compounds, In: Science of Synthesis: Catalytic Oxidation in Organic Synthesis, K. Muniz (Ed.) Reviewed

    Muhammet Uyanik, Kazuaki Ishihara( Role: Joint author ,  Chapter 10)

    Georg Thieme-Verlag: Stuttgart  2017.10  ( ISBN:978-3132012417

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    Total pages:880   Responsible for pages:pp. 635–670   Language:English Book type:Scholarly book

    DOI: 10.1055/sos-SD-225-00320

  5. Asymmetric Oxidative Dearomatization Reaction, In: Asymmetric Dearomatization Reactions, Shu-Li Yu (Ed.) Reviewed

    Muhammet Uyanik, Kazuaki Ishihara( Role: Joint author ,  Chapter 6)

    Wiley-VCH: Weinheim  2016.6  ( ISBN:978-3527338511

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    Total pages:424   Responsible for pages:pp. 129–152   Language:English Book type:Scholarly book

    DOI: 10.1002/9783527698479.ch6

    Other Link: https://www.amazon.com/Asymmetric-Dearomatization-Reactions-Shu-Li-You-dp-3527338519/dp/3527338519/ref=mt_hardcover?_encoding=UTF8&me=&qid=1568806280

  6. Functional Group Transformations via Carbonyl Derivatives, In: Comprehensive Organic Synthesis: 2nd Edition, Gary A. Molander and Paul Knochel (Eds.) Reviewed

    Muhammet Uyanik, Kazuaki Ishihara( Role: Joint author ,  Chapter 6)

    Elsevier: Oxford  2014.4  ( ISBN:9780080977423

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    Total pages:9806   Responsible for pages:pp. 573–597   Language:English Book type:Scholarly book

    DOI: 10.1016/B978-0-08-097742-3.00622-4

    Other Link: https://www.amazon.com/Comprehensive-Organic-Synthesis-Paul-Knochel/dp/0080977421

  7. 2-Iodobenzenesulfonic Acid, In Catalytic Oxidation Reagents, Handbook of Reagents for Organic Chemistry Series, Philip L. Fuchs (ed.) Reviewed International journal

    Muhammet Uyanik, Kazuaki Ishihara, Chi Zhang, Li-Qian Cui( Role: Joint author)

    John Wiley & Sons: Chichester  2013.9  ( ISBN:978-1119953272

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    Total pages:782   Responsible for pages:pp. 332-338   Language:English Book type:Scholarly book

    DOI: 10.1002/047084289X.rn01214.pub2

    Other Link: https://www.amazon.com/Catalytic-Oxidation-Reagents-Philip-Fuchs-dp-1119953278/dp/1119953278/ref=mt_hardcover?_encoding=UTF8&me=&qid=1568807612

  8. 1,2-Benziodoxol-3(1H)-one, 1-Hydroxy, 1-Oxide, In Catalytic Oxidation Reagents, Handbook of Reagents for Organic Chemistry Series, Philip L. Fuchs (ed.) Reviewed International journal

    K. C. Nicolaou, Tamsyn Montagnon, Phil S. Baran, Muhammet Uyanik, Kazuaki Ishihara( Role: Joint author)

    John Wiley & Sons: Chichester  2013.9  ( ISBN:9781119953272

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    Total pages:782   Responsible for pages:pp. 32-48   Language:English Book type:Scholarly book

    DOI: 10.1002/047084289X.rn00236.pub2

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Presentations 281

  1. Hypoiodite-Catalyzed Oxidative Umpolung of Indoles

    Muhammet Uyanik, Hiroki Tanaka, Kazuaki Ishihara

    The 14th Organocatakysis Symposium  

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    Event date: 2021.11

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  2. High-performance Hypohalite Catalysis Invited

    Muhammet Uyanik

    Nagoya University GTR Retreat Seminar 

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    Event date: 2019.6

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Venue:Suzuka Circuit, Mie   Country:Japan  

  3. Development of Environmentally Benign Oxidation Reactions Using Iodine Catalysis Invited

    Muhammet Uyanik

    Green Process Incubation Consortium (GIC) The 59th Seminar 

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    Event date: 2018.12

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Venue:AIST Tohoku Center, Sendai   Country:Japan  

  4. Designer Enantioselective Organoiodine(III) Catalysis Invited

    Muhammet Uyanik

    3rd Workshop on Organic Chemistry, Kyoto University 

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    Event date: 2018.11

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Venue:Kyoto University, Kyoto   Country:Japan  

  5. Hypoiodite Catalysis for Oxidative Coupling Reactions Invited International conference

    Muhammet Uyanik

    The 2nd M&M SYNTHECH Unit International Meeting 2017 

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    Event date: 2017.12

    Language:English   Presentation type:Oral presentation (invited, special)  

    Venue:Nagoya University, Nagoya   Country:Japan  

  6. Enantioselective Hypoiodite Catalysis Invited International conference

    Muhammet Uyanik, Kazuaki Ishihara

    Tateshina Conference in Organic Chemistry 2017 

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    Event date: 2017.11

    Language:English   Presentation type:Poster presentation  

    Venue:Skypark Hotel, Nagano   Country:Japan  

  7. Enantioselective Hypoiodite Catalysis for Oxidative Cyclization Invited International conference

    Muhammet Uyanik

    HALCHEM VIII 

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    Event date: 2017.9

    Language:English   Presentation type:Oral presentation (invited, special)  

    Venue:Meitetsu Inuyama Hotel, Inuyama   Country:Japan  

  8. Development of Selective Oxidation Reactions Using Designer Iodine Catalysts Invited

    Muhammet Uyanik

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:English   Presentation type:Oral presentation (invited, special)  

    Venue:Hiyoshi Campus, Keio University, Yokohama   Country:Japan  

  9. デザイン型ヨウ素触媒による選択的酸化反応 Invited

    Muhammet Uyanik

    特別講演会 

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    Event date: 2017.2

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Venue:岡山大学、岡山   Country:Japan  

  10. Designer Iodine Catalysis for Oxidative Coupling Reactions Invited International conference

    Muhammet Uyanik

    2nd Joint Workshop on Chirality in Chiba University (WCCU) and Soft Molecule Activation (SMA) 

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    Event date: 2016.12

    Language:English   Presentation type:Oral presentation (invited, special)  

    Venue:Chiba University, Chiba   Country:Japan  

  11. Development of Iodine-Based Oxidation Catalysis

    Muhammet Uyanik

    Institute for Molecular Science 

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    Event date: 2016.2

    Language:English   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  12. Catalytic Oxidation Reactions Using Iodine Compounds

    Muhammet Uyanik

    The University of Tokyo Grad. School of Pharmaceutical Sciences, Organic Seminar 

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    Event date: 2015.6

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  13. Catalytic oxidation reactions using iodine compounds International conference

    Muhammet Uyanik

    Anatolian Conference on Synthetic Organic Chemistry (ACSOC-2015) 

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    Event date: 2015.3

    Language:English   Presentation type:Oral presentation (invited, special)  

    Country:Turkey  

  14. Enantioselective Oxidative Dearomatization of Phenols Using Hypervalent Organoiodine Catalysis International conference

    Muhammet Uyanik

    MEXT Canada/Japan Symposium (pre-ISHC) 

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    Event date: 2014.7

    Language:English   Presentation type:Oral presentation (invited, special)  

    Country:Canada  

  15. Chiral Ammonium Hypoiodite Catalysis for Enantioselective Oxidative Cyclization

    7th Symposium of Molecular Activation 

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    Event date: 2014.6

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  16. Enviromentally Benign Synthesis of Biaryl Compounds

    Muhammet Uyanik

    JST Reconstruction Promotion Program A-STEP Matching Event  

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    Event date: 2014.1

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  17. Catalysis with In Situ-Generated (Hypo)iodite Ions for Oxidative Coupling Reactions International conference

    Muhammet Uyanik

    The 4th International Symposium for Young Chemists on Molecular Activation 

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    Event date: 2013.11

    Language:English   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  18. Oxidation Reactions Using Designer Iodine

    Muhammet Uyanik

    The 93rd Annual Meeting of CSJ-Special Program Lecture (Cutting-Edge Organocatalysis) 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  19. Chiral Hypervalent Iodine-Catalyzed Enantioselective Oxidation Reactions

    Muhammet Uyanik

    Joint Seminars 

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    Event date: 2012.4

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  20. Hypervalent Iodine-Catalyzed Enantioselective Oxidative Cyclizations

    Muhammet Uyanik

    92nd Annual Spring Meeting of the Chemical Society of Japan, the Lectureship Award of the Young Generation Special Forum from the CSJ 

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    Event date: 2012.3

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  21. Enantioselective Oxidative Dearomatization of Phenols International conference

    Muhammet Uyanik

    The 1st Nagoya Symposium on Green Synthesis & Catalysis (NSGSC-1) 

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    Event date: 2012.3

    Language:English   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  22. Hypervalent Iodine-Catalyzed Enantioselective Oxidative Cyclizations International conference

    Muhammet Uyanik

    Turkish Chemical Society 25th National Chemistry Congress with International Participation 

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    Event date: 2011.6 - 2011.7

    Language:English   Presentation type:Oral presentation (invited, special)  

    Country:Turkey  

  23. Development of Designer Hypervalent Iodine Catalysis for the Selective Oxidative Transformations

    Muhammet Uyanik

    Organic Seminar of the Tokai Branch of The Society of Synthetic Organic Chemistry, Japan, 2010 

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    Event date: 2010.10

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  24. Oxidative Ritter-type Chloroamidation of Alkenes Using NaCl and Oxone

    Yuto Fujii, Yuya Okada, Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    102nd Annual Spring Meeting of CSJ 

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    Event date: 2022.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  25. Chiral Hypervalent Iodine(III)-catalyzed Enantioselective Oxidative Dearomative Fluorination of Arenols

    Shogo Yamamoto, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    102nd Annual Spring Meeting of CSJ 

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    Event date: 2022.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  26. Enantioselective Dearomative Azidation of Arenols Using Chiral Quaternary Ammonium Hypobromite Catalysis

    Yasuo Tsukimori, Muhammet Uyanik, Kazuaki Ishihara

    102nd Annual Spring Meeting of CSJ 

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    Event date: 2022.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  27. Ammonium Hypoiodite-catalyzed Oxidative Umpolung of Indoles for Dearomatization

    Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    102nd Annual Spring Meeting of CSJ 

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    Event date: 2022.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  28. Cu/I Hybrid Catalysis for Enantioselective Aerobic Coupling Reaction

    Shunki Matsuyama, Soki Ihara, Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    102nd Annual Spring Meeting of CSJ 

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    Event date: 2022.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  29. Chiral Quaternary Ammonium Salt-catalyzed Enantioselective Oxidative Dearomative Chlorination of (Hetero)arenols

    Sachiko Kumagai, Outa Katade, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    102nd Annual Spring Meeting of CSJ 

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    Event date: 2022.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  30. Oxidative Dearomatization of Arenols Using High-performance Hypohalite Catalysis

    Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    102nd Annual Spring Meeting of CSJ 

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    Event date: 2022.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  31. High-performance hypohalite catalysis for enantioselective oxidative dearomatization of arenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Jun-ya Hasegawa, Kazuaki Ishihara

    Nagoya University, GTR Annual Meeting 2021 

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    Event date: 2022.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  32. Development of Chiral Quaternary Ammonium Hypobromite-catalyzed Enantioselective Dearomative Azidation of Arenols

    Yasuo Tsukimori, Muhammet Uyanik, Kazuaki Ishihara

    52nd Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2021.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  33. Development of High-performance Chiral Quaternary Ammonium Salt-catalyzed Enantioselective Dearomative Chlorination of (Hetero)arenols

    Sachiko Kumagai, Outa Katade, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    52nd Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2021.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  34. Hypervalent Iodine(III)-catalyzed Oxidative Dearomative Fluorination of Arenols

    Shogo Yamamoto, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    10th CSJ Chemistry Festa 

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    Event date: 2021.10

    Language:Japanese   Presentation type:Poster presentation  

  35. Ammonium hypoiodite-catalyzed oxidation of indoles towards synthesis of alkaloids

    Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    The 50th Congress of Heterocyclic Chemistry 

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    Event date: 2021.10

    Language:Japanese   Presentation type:Oral presentation (general)  

  36. Oxidative dearomatization of arenols using high-performance hypohalite catalysis

    Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    The 37th Seminar on Synthetic Organic Chemistry 

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    Event date: 2021.9

    Language:Japanese   Presentation type:Poster presentation  

  37. Oxidative dearomatization of arenols using high-performance hypohalite catalysis

    Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    The 24th SIS Symposium 

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    Event date: 2021.9

    Language:Japanese   Presentation type:Poster presentation  

  38. Hypoiodite-catalyzed Chemoselective Oxidative Dearomatization of Indole Derivatives

    Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    The 7th Noyori Forum 

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    Event date: 2021.7

    Language:English   Presentation type:Oral presentation (general)  

  39. Hypoiodite-catalyzed Chemoselective Oxidative Cyclization of Indole Derivatives

    Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    101th Annual Spring Meeting of CSJ 

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    Event date: 2021.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  40. Ring Expansion Reaction of 2-Alkylspiroindolenines via Skeletal Rearrangement to Azepinoindoles

    Toshihiro Yasui, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    101th Annual Spring Meeting of CSJ 

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    Event date: 2021.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  41. Chiral Quaternary Ammonium Hypobromite-catalyzed Enantioselective Dearomative Azidation of Arenols

    Yasuo Tsukimori, Muhammet Uyanik, Kazuaki Ishihara

    101th Annual Spring Meeting of CSJ 

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    Event date: 2021.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  42. High-performance Chiral Quaternary Ammonium Salt-catalyzed Enantioselective Dearomative Chlorination of (Hetero)arenols

    Sachiko Kumagai, Outa Katade, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    101th Annual Spring Meeting of CSJ 

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    Event date: 2021.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  43. Hypervalent Iodine(III)-catalyzed Oxidative Dearomative Fluorination of Arenols

    Shogo Yamamoto, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    101th Annual Spring Meeting of CSJ 

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    Event date: 2021.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  44. Oxidative Dearomatization of Arenols Using High-performance Hypohalite Catalysis

    Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    101th Annual Spring Meeting of CSJ 

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    Event date: 2021.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  45. Enantioselective dearomatization of indoles for total synthesis of natural products

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Toshio Nishikawa, Kazuaki Ishihara

    Nagoya University, GTR Annual Meeting 2019 

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    Event date: 2021.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  46. High-Performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Arenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Junya Hasegawa, Kazuaki Ishihara

    Nagoya University, GTR Annual Meeting 2019 

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    Event date: 2021.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  47. Chiral Quaternary Ammonium Hypobromite Catalysis for Enantioselective Dearomative Azidation of Arenols

    Yasuo Tsukimori, Muhammet Uyanik, Kazuaki Ishihara

    10th CSJ Chemistry Festa 

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    Event date: 2020.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  48. High-Performance Chiral Quaternary Ammonium Salt-Catalyzed Enantioselective Dearomatizative Chlorination of Arenols

    Sachiko Kumagai, Outa Katade, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    10th CSJ Chemistry Festa 

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    Event date: 2020.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  49. Designer quaternary ammonium hypoiodite catalysis for oxidative α-azidation of carbonyl compounds

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  50. Catalytic Skeletal Rearrangement of 2-Alkylspiroindolenines to Azepinoindoles

    Toshihiro Yasui, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  51. Ammonium hypoiodite-catalyzed oxidative umpolung of indoles towards synthesis of alkaloids

    Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  52. Hypoiodite-Catalyzed Chemoselective Oxidative Generation of Quinone Methides and Tandem Reactions

    Ryutaro Kondo, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  53. Chiral Organoiodine(III)-catalyzed Enantioselective Oxidative Biaryl Coupling Reactions

    Shinichi Ishizaki, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  54. Chiral Quaternary Ammonium Hypobromite Catalysis for Enantioselective Dearomative Azidation of Arenols

    Yasuo Tsukimori, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  55. High-Performance Chiral Quaternary Ammonium Salt-Catalyzed Enantioselective Dearomatizative Chlorination of Arenols

    Sachiko Kumagai, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  56. High-Performance Hypoiodite Catalysis for Enantioselective Oxidative Dearomatization of Arenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    100th Annual Spring Meeting of CSJ 

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    Event date: 2020.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  57. Enantioselective dearomatization of indoles for total synthesis of natural products

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Toshio Nishikawa, Kazuaki Ishihara

    Nagoya University, GTR Annual Meeting 2019 

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    Event date: 2020.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  58. High-Performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Arenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Junya Hasegawa, Kazuaki Ishihara

    Nagoya University, GTR Annual Meeting 2019 

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    Event date: 2020.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  59. Hypoiodite-catalyzed Chemoselective Oxidative Generation of ortho-Quinone Methides and Tandem Reactions

    Muhammet Uyanik

    The 12th Organocatalysis Symposium 

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    Event date: 2019.12

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Kyoto University   Country:Japan  

  60. High-performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Phenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    50th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2019.11

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Shinshu University Matsumoto Campus, Nagano   Country:Japan  

  61. Ring Expansion Reaction of 2-Alkylspiroindolenines via 1,3-Rearrangement to Azepinoindoles

    Toshihiro Yasui, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    9th CSJ Chemistry Festa 

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    Event date: 2019.10

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Tower Hall Funabori, Tokyo   Country:Japan  

  62. Practical Scalability of Chiral Organoiodine(III)-catalyzed Enantioselective Oxidation Reactions

    Shinichi Ishizaki, Muhammet Uyanik, Kazuaki Ishihara

    9th CSJ Chemistry Festa 

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    Event date: 2019.10

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Tower Hall Funabori, Tokyo   Country:Japan  

  63. Umpolung of Indoles for Catalytic Enantioselective Dearomatization Reactions

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 36th Seminar on Organic Chemistry 

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    Event date: 2019.9

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagarawa Convention Center, Gifu   Country:Japan  

  64. High-performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Phenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 36th Seminar on Organic Chemistry 

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    Event date: 2019.9

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagarawa Convention Center, Gifu   Country:Japan  

  65. Hypoiodite-catalyzed Chemoselective Oxidative Generation of ortho-Quinone Methides and Tandem Reactions International conference

    Muhammet Uyanik, Kohei Nishioka, Kazuaki Ishihara

    The 27th International Society of Heterocyclic Chemistry Congress (ISHC) 

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    Event date: 2019.9

    Language:English   Presentation type:Poster presentation  

    Venue:Miyako Messe, Kyoto   Country:Japan  

  66. IBS-catalyzed Highly Efficient and Selective Oxidation of Alcohols with Oxone International conference

    Ryutaro Kondo, Muhammet Uyanik, Kazuaki Ishihara

    The 27th International Society of Heterocyclic Chemistry Congress (ISHC) 

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    Event date: 2019.9

    Language:English   Presentation type:Poster presentation  

    Venue:Miyako Messe, Kyoto   Country:Japan  

  67. Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Indoles

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

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    Event date: 2019.8

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  68. Chiral Hypoiodite-catalyzed Umpolung of Indoles for Enantioselective Dearomatization

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 22nd SIS Symposium 

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    Event date: 2019.8

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Chiba University, Chiba   Country:Japan  

  69. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Indoles

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 54th Natural Product Chemistry Seminar 

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    Event date: 2019.7

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Jozankei Onsen Hotel Shikanoyu, Sapporo   Country:Japan  

  70. Scalability of Chiral Organoiodine(III)-catalyzed Enantioselective Oxidation Reactions

    Shinichi Ishizaki, Muhammet Uyanik, Kazuaki Ishihara

    The 54th Summer School of Organic Reaction Society 

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    Event date: 2019.6 - 2019.7

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Marine Lodge Kaifukan, Osaka   Country:Japan  

  71. Ring Expansion Reaction of 2-Alkylspiroindolenines via 1,3-Rearrangement to Azepinoindoles

    Toshihiro Yasui, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    The 52nd Summer School of Organometallic Chemistry Society 

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    Event date: 2019.6

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Setouchi Kojima Hotel, Kurashiki, Okayama   Country:Japan  

  72. High-Performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Phenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 52nd Summer School of Organometallic Chemistry Society 

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    Event date: 2019.6

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Setouchi Kojima Hotel, Kurashiki, Okayama   Country:Japan  

  73. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Indoles

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University GTR Retreat Seminar 

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    Event date: 2019.6

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Suzuka Circuit, Mie   Country:Japan  

  74. High-Performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Phenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University GTR Retreat Seminar 

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    Event date: 2019.6

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Suzuka Circuit, Mie   Country:Japan  

  75. IBS-catalyzed Highly Efficient and Selective Oxidation and Oxidative Esterification of Alcohols with Oxone

    Ryutaro Kondo, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  76. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Indoles

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  77. Ring Expansion Reaction of 2-Alkylspiroindolenines via 1,3-Rearrangement to Azepinoindoles

    Toshihiro Yasui, Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  78. Scalability of Chiral Organoiodine(III)-catalyzed Enantioselective Oxidation Reactions

    Shinichi Ishizaki, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  79. Chiral Hypoiodite-catalyzed Enantioselective Oxidative α-Azidation of Carbonyl Compounds

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  80. Chiral Quaternary Ammonium Salt-catalyzed Enantioselective Oxidative Dearomatizative Chlorination of Naphthols

    Outa Katade, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  81. High-Performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Phenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  82. Hypoiodite-catalyzed Chemoselective Generation of Quinone Methides and Application to Tandem Reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 99th Annual Meeting of CSJ  

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    Event date: 2019.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Konan University (Okamoto Campus), Hyogo   Country:Japan  

  83. Chiral Hyproiodite-catalyzed Enantioselective Oxidative α-Azidation of Carbonyl Compounds

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University IGER Annual Meeting 2018 

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    Event date: 2019.1

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  84. Hypoiodite-catalyzed Chemoselective Generation of Quinone Methides and Application to Tandem Reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University IGER Annual Meeting 2018 

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    Event date: 2019.1

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  85. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Indoles

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    Kickoff Meeting of Nagoya University Gradute Program of Transformative Chem-Bio Research (GTR) 

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    Event date: 2019.1

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nagoya University, Nagoya   Country:Japan  

  86. High-Performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Phenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    Kickoff Meeting of Nagoya University Gradute Program of Transformative Chem-Bio Research (GTR) 

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    Event date: 2019.1

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nagoya University, Nagoya   Country:Japan  

  87. High-Performance Hypohalite Catalysis for Enantioselective Oxidative Dearomatization of Phenols

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    IGER/ITbM Chemistry Workshop 2018 

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    Event date: 2018.12

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nagoya University, Nagoya   Country:Japan  

  88. Indole Umpolung Directed Enantioselective Oxidative Cyclization

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    49th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2018.11

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  89. Chemoselective Oxidation of Phenols to Quinone Methides and Application to Tandem Reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    49th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2018.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nagoya University, Nagoya   Country:Japan  

  90. Chiral Hypohalite-catalyzed Enantioselective Dearomatizative Spirolactonization of Phenol Derivatives

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 8th CSJ Chemistry Festa 

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    Event date: 2018.10

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Tower Hall Funabori, Tokyo   Country:Japan  

  91. Hypervalent Organoiodine(V)-catalyzed Highly Efficient and Selective Oxidation of Alcohols

    Ryutaro Kondo, Muhammet Uyanik, Kazuaki Ishihara

    The 8th CSJ Chemistry Festa 

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    Event date: 2018.10

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Tower Hall Funabori, Tokyo   Country:Japan  

  92. Hyproiodite-catalyzed Direct α-Azidation of Carbonyl Compounds

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

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    Event date: 2018.9

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  93. Enantioselective Hypoiodite Catalysis for Oxidative Coupling Reactions International conference

    Muhammet Uyanik, Hiroki Hayashi, Daisuke Suzuki, Hirokazu Iwata, Kazuaki Ishihara

    The 4th International Symposium on C-H Activation (ISCHA4) 

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    Event date: 2018.8 - 2018.9

    Language:English   Presentation type:Poster presentation  

    Venue:Keio University, Hiyoshi Campus, Yokohama   Country:Japan  

  94. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Indol Derivatives

    Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    The 53th Seminar on Natural Products Chemistry  

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    Event date: 2018.7

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Ikeda, Osaka   Country:Japan  

  95. Hypervalent Organoiodine(V)-catalyzed Highly Efficient and Selective Oxidation of Alcohols

    Ryutaro Kondo, Muhammet Uyanik, Kazuaki Ishihara

    The 53th Natural Product Chemistry Seminar 

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    Event date: 2018.7

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Ikeda, Osaka   Country:Japan  

  96. Chiral Hypohalite-catalyzed Enantioselective Dearomatizative Spirolactonization of Phenol Derivatives

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 51th Summer School of Organometallic Chemistry Society  

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    Event date: 2018.7

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Kyoto   Country:Japan  

  97. High Performance Hypoiodite Catalysis for Oxidative α-Azidation of Carbonyl Compounds

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 113th Organic Synthesis Symposium of The Society of Synthetic Organic Chemistry, Japan  

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    Event date: 2018.6

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Sakata-Hirata Hall   Country:Japan  

  98. Chiral Hypoiodite-catalyzed Enantioselective Synthesis of Spiroindolenines

    Hiroki Tanaka, Muhammet Uyanik, Kazuaki Ishihara

    The 113th Organic Synthesis Symposium of The Society of Synthetic Organic Chemistry, Japan  

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    Event date: 2018.6

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Sakata-Hirata Hall   Country:Japan  

  99. Chiral Hypoiodite-catalyzed Enantioselective Cascade Aminocyclization to 2-Acylpiperazines

    Hirokazu Iwata, Muhammet Uyanik, Kazuaki Ishihara

    The 98th Annual Meeting of CSJ  

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    Event date: 2018.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nihon University Funabashi Campus, Chiba   Country:Japan  

  100. Chiral Hypoiodite-catalyzed enantioselective oxidative aminospirocyclization of indole derivatives

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 98th Annual Meeting of CSJ  

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    Event date: 2018.3

    Language:English   Presentation type:Oral presentation (general)  

    Venue:Nihon University Funabashi Campus, Chiba   Country:Japan  

  101. Chiral Hypohalite-catalyzed Enantioselective Dearomatizative Spirolactonization

    Takehiro Kato, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 98th Annual Meeting of CSJ  

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    Event date: 2018.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nihon University Funabashi Campus, Chiba   Country:Japan  

  102. Chiral Hypohalite-catalyzed Enantioselective Dearomatizative Cycloamination

    Outa Katade, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 98th Annual Meeting of CSJ  

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    Event date: 2018.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nihon University Funabashi Campus, Chiba   Country:Japan  

  103. Hypoiodite-catalyzed Oxidative α-Azidation of Carbonyl Compounds

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 98th Annual Meeting of CSJ  

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    Event date: 2018.3

    Language:English   Presentation type:Oral presentation (general)  

    Venue:Nihon University Funabashi Campus, Chiba   Country:Japan  

  104. Hypervalent Organoiodine(V)-catalyzed Highly Efficient and Selective Oxidation of Alcohols

    Ryutaro Kondo, Muhammet Uyanik, Kazuaki Ishihara

    The 98th Annual Meeting of CSJ  

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    Event date: 2018.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Nihon University Funabashi Campus, Chiba   Country:Japan  

  105. Hypoiodite-catalyzed Oxidative Generation of Quinone Methides and Application to Tandem Reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 98th Annual Meeting of CSJ  

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    Event date: 2018.3

    Language:English   Presentation type:Oral presentation (general)  

    Venue:Nihon University Funabashi Campus, Chiba   Country:Japan  

  106. Hypoiodite-catalyzed Oxidative Generation of Quinone Methides and Application to Tandem Reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University, IGER Annual Meeting 2017 

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    Event date: 2018.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  107. Chiral Hypoiodite Catalysis for Enantioselective Oxidative Dearomatization of Indole Derivatives

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University, IGER Annual Meeting 2017 

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    Event date: 2018.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  108. Hypoiodite-catalyzed oxidative α-azidation of carbonyl compounds

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University, IGER Annual Meeting 2017 

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    Event date: 2018.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  109. Hypoiodite-catalyzed Chemoselective Direct α-Azidation of Carbonyl Compounds International conference

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    1st Singapore Japan Germany Trilateral Symposium on Precision Synthesis & Catalysis 

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    Event date: 2017.11

    Language:English   Presentation type:Poster presentation  

    Venue:Nanyang Technological University, Singapore   Country:Singapore  

  110. Chiral Hypoiodite-catalyzed Enantioselective Oxidative DEaromatization of Indoles

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 7th CSJ Chemistry Festa 

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    Event date: 2017.10

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Tower Hall Funabori, Tokyo   Country:Japan  

  111. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Cascade Cyclization

    Hirokazu Iwata, Muhammet Uyanik, Kazuaki Ishihara

    The 7th CSJ Chemistry Festa 

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    Event date: 2017.10

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:Tower Hall Funabori, Tokyo   Country:Japan  

  112. Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Phenols International conference

    Outa Katade, Naoto Sahara, Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    HALCHEM VIII 

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    Event date: 2017.9

    Language:English   Presentation type:Poster presentation  

    Venue:Meitetsu Inuyama Hotel, Inuyama   Country:Japan  

  113. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Cascade Cyclization International conference

    Hirokazu Iwata, Muhammet Uyanik, Kazuaki Ishihara

    HALCHEM VIII 

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    Event date: 2017.9

    Language:English   Presentation type:Poster presentation  

    Venue:Meitetsu Inuyama Hotel, Inuyama   Country:Japan  

  114. Hypoiodite-catalyzed Chemoselective Direct α-Azidation of Carbonyl Compounds International conference

    Naoto Sahara, Yuhei Hattori, Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    HALCHEM VIII 

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    Event date: 2017.9

    Language:English   Presentation type:Poster presentation  

    Venue:Meitetsu Inuyama Hotel, Inuyama   Country:Japan  

  115. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Indole Derivatives International conference

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    HALCHEM VIII 

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    Event date: 2017.9

    Language:English   Presentation type:Poster presentation  

    Venue:Meitetsu Inuyama Hotel, Inuyama   Country:Japan  

  116. Chiral Hypoiodite-catalyzed Enantioselective Synthesis of Azaspiroindolenine Derivatives

    Hiroki Tanaka, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 20th SIS Symposium 

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    Event date: 2017.9

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Chiba University, Chiba   Country:Japan  

  117. Chiral Hypoiodite-catalyzed Enantioselective Synthesis of Azaspiroindolenine Derivatives

    Hiroki Tanak, Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 50th Summer School of Organometallic Chemistry Society  

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    Event date: 2017.8

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  118. Hypoiodite Catalysis for Oxidative α-Azidation of Carbonyl Compounds

    Naoto Sahara, Yuhei Hattori, Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    JSPC2017 Summer Symposium 

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    Event date: 2017.8

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  119. Hypoiodite Catalysis for Oxidative α-Azidation of Carbonyl Compounds

    Naoto Sahara, Yuhei Hattori, Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 52nd Summer School of Organic Reaction Society  

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    Event date: 2017.7

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  120. Hypoiodite-catalyzed Enantio- and Chemoselective Oxidative Dearomatization of Phenols

    Outa Katade, Naoto Sahara, Takehiro Kato, Muhammet Uyanik, Kazuaki Ishihara

    The 52nd Seminar on Natural Products Chemistry  

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    Event date: 2017.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  121. High-Performance Hypoiodite Catalysis for Oxidative α-Azidation of Carbonyl Compounds

    Naoto Sahara, Yuhei Hattori, Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  122. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization to Azaspiroindolenine Derivatives

    Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  123. Chiral Hypervalent Iodine(III)-catalyzed Enantioselective Oxidative Spirolactonization of Biaryl Hydroxy Carboxylic Acids

    Kirara Saeda, Muhammet Uyanik, Kazuaki Ishihara

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  124. Hypoiodite-catalyzed Oxidative Tandem Reactions via ortho-Quinone Methides

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  125. IBS-Catalyzed Site-selective Oxidation of Phenols to 1,2-Quinols

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  126. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Cascade Cyclization

    Hirokazu Iwata, Muhammet Uyanik, Kazuaki Ishihara

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  127. Chiral Hypoiodite-catalyzed Enantioselective Oxidative Dearomatization of Phenols

    Outa Katade, Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 97th Annual Meeting of CSJ  

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    Event date: 2017.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  128. Hypoiodite-catalyzed Oxidative Tandem Reactions via ortho-Quinone Methides

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University, IGER Annual Meeting 2016 

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    Event date: 2017.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  129. Chiral hypervalent iodine(III)-catalyzed enantioselective oxidative dearomatization of biaryl hydroxy carboxylic acids

    Kirara Saeda, Muhammet Uyanik, Kazuaki Ishihara

    47th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2016.11

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Toyohashi University of Technology, Aichi   Country:Japan  

  130. Hypoiodite-catalyzed oxidative α-azidation of carbonyl compounds

    Naoto, Sahara, Yuhei Hattori, Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 9th Fluorous Science Symposium 

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    Event date: 2016.10

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  131. Hypoiodite-Catalyzed Peroxidative Dearomatization of Phenols

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 19th SIS Symposium 

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    Event date: 2016.9

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Chiba University, Chiba   Country:Japan  

  132. Hypoiodite-catalyzed Peroxidative Dearomatization of Phenols

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

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    Event date: 2016.8

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  133. Practical and Efficient Oxidation and Chlorination Reactions Using Sodium Hypochlorite Pentahydrate Invited International conference

    Muhammet Uyanik, Kazuaki Ishihara, Mitsuyoshi Kuwahata, Yasukazu Ejima

    JSPC 2016 Summer Symposium 

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    Event date: 2016.7

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya Congress Center, Aichi   Country:Japan  

  134. Hypoiodite-Catalyzed Peroxidative Dearomatization of Phenols

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 51th Summer School of Organic Reaction Society  

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    Event date: 2016.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  135. Chiral hypoiodite-catalyzed enantioselective oxidative cycloetherification

    Hirokazu Iwata, Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 51th Summer School of Organic Reaction Society 

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    Event date: 2016.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  136. Hypoiodite-catalyzed α-azidation of carbonyl compounds

    Naoto, Sahara, Yuhei Hattori, Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 51th Seminar on Natural Products Chemistry  

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    Event date: 2016.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  137. Oxidative generation of ortho-quinone methides and application to tandem reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  138. Chiral hypoiodite-catalyzed enantioselective oxidative cycloetherification

    Hirokazu Iwata, Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  139. Chiral hypervalent iodine(III)-catalyzed enantioselective oxidative dearomatization of 1,4-hydroquinone derivatives

    Masahiro Mizuno, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  140. Chiral hypervalent iodine(III)-catalyzed oxidative kinetic resolution of biaryl hydroxy carboxylic acids

    Kirara Saeda, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  141. IBS-catalyzed regioselective oxidation of phenols and its synthetic application

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  142. Chiral hypoiodite-catalyzed enantioselective oxidative dearomatization of indole derivatives

    Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  143. Development of oxidative dearomatization reaction using hypochlorite salt catalysts

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  144. Hypoiodite-catalyzed oxidative α-azidation of carbonyl compounds

    Yuhei Hattori, Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  145. Catalytic α-chlorination of carbonyl compounds with sodium hypochlorite pentahydrate

    Fumio Nakashima, Muhammet Uyanik, Kazuaki Ishihara, Mitsuyoshi Kuwahata, Yasukazu Ejima

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  146. Chiral hypoiodite-catalyzed enantioselective oxidative cyclization and mechanistic study

    Hiroki Hayashi, Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    The 96th Annual Meeting of CSJ  

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    Event date: 2016.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  147. IBS-Catalyzed Regioselective Oxidation of Phenols to 1,2-Quinols and Its Synthetic Application

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University, IGER Annual Meeting 2015 

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    Event date: 2016.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  148. Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Cyclization and Mechanistic Study

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya University, IGER Annual Meeting 2015 

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    Event date: 2016.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  149. IBS-Catalyzed Regioselective Oxidation of Phenols and Its Synthetic Application

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

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    Event date: 2015.11

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  150. ortho-キノンメチドの新規酸化的生成及びタンデム型反応への応用

    西岡浩平, UYANIK Muhammet, 石原一彰

    名古屋大学グリーン自然科学国際教育研究プログラム・分子科学研究所リトリート研修「分子研め知られざる有機合成の世界」 

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    Event date: 2015.11

    Language:Japanese   Presentation type:Poster presentation  

    Venue:分子科学研究所(岡崎)   Country:Japan  

  151. 次亜ヨウ素酸触媒を用いるカルボニル化合物の酸化的α−ハロゲン化反応

    佐原直登, UYANIK Muhammet, 石原一彰

    名古屋大学グリーン自然科学国際教育研究プログラム・分子科学研究所リトリート研修「分子研め知られざる有機合成の世界」 

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    Event date: 2015.11

    Language:Japanese   Presentation type:Poster presentation  

    Venue:分子科学研究所(岡崎)   Country:Japan  

  152. IBS-catalyzed ortho-Selective Oxidation of Phenols to 1,2-Quinols

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

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    Event date: 2015.9

    Language:Japanese   Presentation type:Poster presentation  

    Venue:Nagoya University, Nagoya   Country:Japan  

  153. 高活性キラル次亜ヨウ素酸塩触媒を用いるクロマンの不斉合成

    UYANIK Muhammet, 石原一彰

    テクノ・フェア名大2015 

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    Event date: 2015.9

    Language:Japanese   Presentation type:Poster presentation  

    Venue:名古屋大学   Country:Japan  

  154. Deevelopment of Oxidative In situ Generation of ortho-Quinone Methides and Cascade Reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 50th Summer School of Organic Reaction Society 

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    Event date: 2015.7

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  155. Deevelopment of Oxidative In situ Generation of ortho-Quinone Methides and Cascade Reactions

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 50th Summer School of Organic Reaction Society 

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    Event date: 2015.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  156. Oxidative a-Halogenation of Carbonyl Compounds Using Hypoiodite Catalysis

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 48th Summer School of Organometallic Chemistry Society 

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    Event date: 2015.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  157. Oxidative Enantiomeric Discrimination of Biphenols Induced by Chiral Hypervalent Iodine(Ⅲ) Catalysts

    Kirara Saeda, Muhammet Uyanik, Kazuaki Ishihara

    The 50th Seminar on Natural Products Chemistry  

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    Event date: 2015.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  158. Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Dearomatization of Indole Derivatives

    Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 50th Seminar on Natural Products Chemistry 

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    Event date: 2015.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  159. IBS-Catalyzed ortho-Selective Oxidation of Phenols to 1,2-Quinols

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 107th Organic Synthesis Symposium 

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    Event date: 2015.6

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  160. Site- and Enantioselective Oxidative Cycloamination Using Chiral Hypoiodite Catalysis

    Muhammet Uyanik, Daisuke Suzuki, Kazuaki Ishihara

    CREST "High-performance Nanostructure Materials" The 5th Symposium 

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    Event date: 2015.6

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  161. Practical Oxidative Dearomatization of Phenols with Sodium Hypochlorite Pentahydrate

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara, Mitsuyoshi Kuwahata, Yasukazu Ejima

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  162. Site- and Enantioselective Oxidative Cycloamination Using Chiral Hypoiodite Catalysis

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  163. Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Cyclization to Alicyclic Ethers

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  164. IBS-Catalyzed ortho-Selective Oxidation of Phenols to 1,2-Quinols

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  165. Oxidative Enantiomeric Discrimination of Biphenols Induced by Chiral Hypervalent Iodine(Ⅲ) Catalysts

    Kirara Saeda, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  166. a-Oxidative C-N Coupling Reaction of Carbonyl Compounds Using Hypoiodite Catalysis

    Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  167. Oxidative a-Chlorination of Carbonyl Compounds Using Hypoiodite Catalysis

    Naoto Sahara, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  168. Chiral Iodine(I or III)-Catalyzed Oxidative Dearomatization of Phenols

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  169. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Spirolactonization of (4-Hydroxyphenyl)carboxylic Acid Derivatives

    Masahiro Mizuno, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  170. Hypoiodite-Catalyzed Oxidative Hetero-Diels-Alder Reaction of Phenols

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  171. Hypoiodite-Catalyzed Oxidative Dearomatization of Indole Derivatives

    Naoya Ukegawa, Muhammet Uyanik, Kazuaki Ishihara

    The 95th Annual Meeting of CSJ  

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    Event date: 2015.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  172. Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Cycloamination

    Daisuke Suzuki, Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    45th Annual Meeting of Union of Chemistry-Related Societies 

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    Event date: 2014.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  173. High-Turnover Hypoiodite Catalysis for the Enantioselective Synthesis of Tocopherols

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 31st Seminar on Synthetic Organic Chemistry 

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    Event date: 2014.9

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  174. Design of Quaternary Perfluoroammonium Iodide Catalysts: Enantioselective Oxidative Coupling Reactions

    Kazuaki Ishihara, Muhammet Uyanik, Daisuke Suzuki, Hiroki Hayashi

    The 7th Symposium of the Society of Fluorous Science 

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    Event date: 2014.9

    Language:Japanese   Presentation type:Oral presentation (invited, special)  

    Country:Japan  

  175. Enantioselective Synthesis of Tocopherols Using Chiral Ammonium Hypoiodite Catalysis

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    Sympsosium of Medicinal Sciences in Gifu 2014 

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    Event date: 2014.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  176. Hypervalent Iodine(V)-Catalyzed ortho-Selective Oxidation of Phenols with Oxone to 1,2-Quinols and Application to Natural Product Synthesis

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    Sympsosium of Medicinal Sciences in Gifu 2014 

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    Event date: 2014.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  177. High-Turnover Hypoiodite Catalysis of Enantioselective Oxidative Cycloetherification to Synthesize Optically Active Tocopherols International conference

    Muhammet Uyanik, Hiroki Hayashi, Kazuaki Ishihara

    The 19th International Symposium on Homogeneous Catalysis (ISHC-XIX) 

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    Event date: 2014.7

    Language:English   Presentation type:Oral presentation (general)  

    Country:Canada  

  178. IBS-Catalyzed ortho-Selective Oxidation of Phenols to 1,2-Quinols International conference

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 4th International Conference on Hypervalent Iodine Chemistry (ICHIC2014) 

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    Event date: 2014.7

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  179. Hypervalent Organoiodine Catalysis for Enantioselective Oxidative Dearomatization of Phenols International conference

    Muhammet Uyanik, Takeshi Yasui, Niiha Sasakura, Kazuaki Ishihara

    The 4th International Conference on Hypervalent Iodine Chemistry (ICHIC2014) 

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    Event date: 2014.7

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  180. Chiral Ammonium Hypoiodite Catalysis for Enantioselective Oxidative Cycloamination International conference

    Daisuke Suzuki, Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    The 4th International Conference on Hypervalent Iodine Chemistry (ICHIC2014) 

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    Event date: 2014.7

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  181. Enantioselective Synthesis of ortho-Benzoquinone Monoacetals Using Chiral Hypervalent Organoiodine(III)-Catalysts International conference

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    The 4th International Conference on Hypervalent Iodine Chemistry (ICHIC2014) 

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    Event date: 2014.7

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  182. Enantioselective Synthesis of Tocopherols Using Chiral Ammonium Hypoiodite Catalysis International conference

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 4th International Conference on Hypervalent Iodine Chemistry (ICHIC2014) 

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    Event date: 2014.7

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  183. Dearomatizative Epoxidation of Phenol Derivatives Using Hypoiodite Salt Catalysts

    Kohei Nishioka, Muhammet Uyanik, Kazuaki Ishihara

    The 49th Seminar on Natural Products Chemistry 

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    Event date: 2014.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  184. Hypervalent Iodine(V)-Catalyzed ortho-Selective Oxidation of Phenols with Oxone to 1,2-Quinols

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ  

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  185. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols to 2,5-Cyclohexadienones

    Masahiro Mizuno, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ  

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  186. Oxidative Dearomatization of Phenol Derivatives Using Hypoiodite Salt Catalysts

    Kohei Nishioka, Kento Ohori, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ  

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  187. Oxidative α-Imidation and α-Azidation of Carbonyl Compounds Using Hypoiodite Catalysis

    Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ 

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  188. Synthesis of Arylquinones from Hydroquinones Using Tandem One-Pot Oxidation/Cross Coupling Reactions

    Dai Nagata, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ  

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    Event date: 2014.3

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  189. Synthesis of Arylquinones from Hydroquinones Using Tandem One-Pot Oxidation/Cross Coupling Reactions

    Dai Nagata, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ  

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  190. Synthesis of Biologically Active Compounds Using Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Cycloamination

    Daisuke Suzuki, Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ 

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  191. Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Cycloetherification to 2-Acylchromans and Investigation of Catalytic Mechanism

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ 

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  192. Chiral Hypervalent Iodine(III) Catalysis for Enantioselective Synthesis of ortho-Benzoquinone Monoacetals

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    The 94th Annual Meeting of CSJ 

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    Event date: 2014.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  193. Chiral Hypervalent Iodine(III) Catalysis for Enantioselective Synthesis of ortho-Benzoquinone Monoacetals

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2013 

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    Event date: 2014.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  194. Synthesis of Biologically Active Compounds Using Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Cycloamination

    Daisuke Suzuki, Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2013 

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    Event date: 2014.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  195. Hypervalent Iodine(V)-Catalyzed ortho-Selective Oxidation of Phenols with Oxone to 1,2-Quinols

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2013 

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    Event date: 2014.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  196. Chiral Hypoiodite-Catalyzed Enantioselective Oxidative Cycloetherification to 2-Acylchromans and Investigation of Catalytic Mechanism

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2013 

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    Event date: 2014.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  197. Hydrogen Bonding and Alcohol Effects in Asymmetric Hypervalent Organoiodine Catalysis: Enantioselective Oxidative Dearomatization of Phenols International conference

    Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara

    The 8th International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOCA-8 & NICCEOCA-4) 

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    Event date: 2013.11

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  198. Enantioselective Oxidative Cycloamination Catalyzed by Chiral (Hypo)iodite Species

    Daisuke Suzuki, Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    The 3rd CSJ Chemistry Festa 

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    Event date: 2013.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  199. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols to ortho-Benzoquinone Monoacetals

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    The 3rd CSJ Chemistry Festa 

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    Event date: 2013.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  200. (Hypo)Iodite-Catalyzed Oxidative Carbon-Nitrogen Coupling Reaction at alpha-Position of Ketones

    Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 16th Symposium of the Society of Iodine Science  

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    Event date: 2013.9

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  201. (Hypo)Iodite-Catalyzed Oxidative Carbon-Nitrogen Coupling Reaction at alpha-Position of Ketones International conference

    Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 48th Summer School of Organic Reaction Society 

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    Event date: 2013.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  202. (Hypo)iodite-Catalyzed Oxidative Biaryl Coupling Reaction of Phenols

    Dai Nagata, Muhammet Uyanik, Kazuaki Ishihara

    The 48th Summer School of Organic Reaction Society 

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    Event date: 2013.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  203. Hypervalent Iodine(V)-Catalyzed Regioselective Oxidation of Phenols with Oxone

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 46th Summer School of Organometallic Chemistry Society  

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    Event date: 2013.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  204. Enantioselective Synthesis of 2-Acylchroman Derivatives Using Chiral (Hypo)iodite Catalysts

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 48th Seminar on Natural Products Chemistry 

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    Event date: 2013.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  205. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols to ortho-Benzoquinone Monoacetals

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    48th Summer School of Chemistry of Natural Product 

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    Event date: 2013.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  206. Enantioselective Oxidative Cycloamination Catalyzed by Chiral (Hypo)iodite Species

    Daisuke Suzuki, Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    The 48th Seminar on Natural Products Chemistry 

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    Event date: 2013.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  207. Enantioselective Synthesis of 2-Acylchroman Derivatives Using Chiral (Hypo)iodite Catalysts International conference

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya Symposium 2013 

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    Event date: 2013.5

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  208. Enantioselective Oxidative Cycloamination Catalyzed by Chiral (Hypo)iodite Species International conference

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya Symposium 2013 

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    Event date: 2013.5

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  209. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols to ortho-Benzoquinone Monoacetals International conference

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    Nagoya Symposium 2013 

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    Event date: 2013.5

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  210. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols and the Reaction Mechanism

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Isihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  211. Hypervalent Iodine(V)-Catalyzed Regioselective Oxidation of Phenols with Oxone and Its Synthetic Application

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  212. (Hypo)Iodite-Catalyzed Oxidative Carbon-Nitrogen Coupling Reaction at alpha-Position of Ketones

    Mayuko Tsukahara, Muhammet Uyanik, Kazuaki Ishihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  213. (Hypo)iodite-Catalyzed Oxidative Biaryl Coupling Reaction of Phenols

    Dai Nagata, Muhammet Uyanik, Kazuaki Ishihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  214. Chiral (Hypo)iodite-Catalyzed Enantioselective Oxidative Dearomatization of 1-Naphthol Derivatives

    Kento Ohori, Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  215. Enantioselective Synthesis of 2-Acylchroman Derivatives Using Chiral (Hypo)iodite Catalysts

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  216. Enantioselective Oxidative Cycloamination Catalyzed by Chiral (Hypo)iodite Species

    Daisuke Suzuki, Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  217. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols to ortho-Benzoquinone Monoacetals

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    The 93rd Annual Meeting of CSJ 

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    Event date: 2013.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  218. Enantioselective Synthesis of 2-Acylchroman Derivatives Using Chiral (Hypo)iodite Catalysts

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2012 

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    Event date: 2013.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  219. Enantioselective Oxidative Cycloamination Catalyzed by Chiral (Hypo)iodite Species

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2012 

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    Event date: 2013.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  220. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols to ortho-Benzoquinone Monoacetals

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2012 

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    Event date: 2013.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  221. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenol Derivatives

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2012 

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    Event date: 2013.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  222. IBS-Catalyzed Regioselective Oxidation of Phenols with Oxone

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    IGER Annual Meeting 2012 

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    Event date: 2013.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  223. Baeyer-Villiger Oxidation and Oxidative Cascade Reactions with Aqueous Hydrogen Peroxide Catalyzed by Lipophilic Li[B(C6F5)4] or Ca[B(C6F5)4]2 International conference

    Muhammet Uyanik, Daisuke Nakashima, Kazuaki Ishihara

    The 7th International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOCA-7/NICCEOCA-3) 

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    Event date: 2012.12

    Language:English   Presentation type:Poster presentation  

    Country:Singapore  

  224. Highly Efficient and Selective Baeyer-Villiger Oxidation with Aqueous Hydrogen Peroxide Catalyzed by LiB(C6F5)4 or Ca[B(C6F5)4]2 International conference

    Kazuaki Ishihara, Muhammet Uyanik, Daisuke Nakashima

    The 12th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-12) 

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    Event date: 2012.11

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  225. Chiral (Hypo)iodite-Catalyzed Enantioselective Intramolecular Oxidative Coupling Reactions Directed toward 2-Acylchroman Derivatives

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    43rd Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2012.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  226. Baeyer-Villiger Oxidation with Hydrogen Peroxide Using Lipophilic Catalysis

    Muhammet Uyanik, Kazuaki Ishihara

    10th Forum of Sekisui Chemical Innovations Inspired by Nature 

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    Event date: 2012.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  227. IBS-Catalyzed Selective Oxidation of Phenols to 1,2-Quinones with Oxone

    Muhammet Uyanik, Tatsuya Mutsuga, Kazuaki Ishihara

    The 15th Symposium of the Society of Iodine Science 

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    Event date: 2012.9

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  228. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of Phenols

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    The 29th Seminar on Synthetic Organic Chemistry 

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    Event date: 2012.9

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  229. Chiral (Hypo)iodite Catalyzed Enantioselective Intramolecular Oxidative Etherification to 2-Acylchroman Derivatives

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    2012 Summer Symposium of the Japanese Society for Process Chemistry 

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    Event date: 2012.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  230. Chiral Hypervalent Iodine Catalysis for Enantioselective Oxidative Dearomatization of Phenols International conference

    Muhammet Uyanik

    The 59th Organic Reactions and Processes Gordon Research Conference 

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    Event date: 2012.7

    Language:English   Presentation type:Poster presentation  

    Country:United States  

  231. IBS-Catalyzed Oxidation of Phenols with Oxone

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    The 45th Summer School of Organometallic Chemistry Society 

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    Event date: 2012.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  232. Chiral Hypervalent Iodine-Catalyzed Enantioselective Oxidative Dearomatization of Phenol Derivatives

    Niiha Sasakura, Muhammet Uyanik, Kazuaki Ishihara

    The 45th Summer School of Organometallic Chemistry Society 

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    Event date: 2012.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  233. Chiral (Hypo)iodite Catalyzed Enantioselective Intramolecular Oxidative Etherification to 2-Acylchroman Derivatives

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    The 47th Seminar on Natural Products Chemistry 

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    Event date: 2012.7

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  234. (Hypo)iodite-Catalyzed Oxidative Biaryl Coupling of Phenols with Hydrogen Peroxide

    Dai Nagata, Muhammet Uyanik, Kazuaki Ishihara

    The 1st JACI/GSC Symposium 

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    Event date: 2012.6

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  235. Chiral (Hypo)iodite Catalyzed Enantioselective Intramolecular Oxidative Etherification to 2-Acylchroman Derivatives

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    92th Annual Spring Meeting of CSJ 

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    Event date: 2012.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  236. Alkali or Alkaline Earth Metal Bulky Borate Salt Catalysis for Baeyer-Villiger Oxidation with Hydrogen Peroxide

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    92th Annual Spring Meeting of CSJ 

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    Event date: 2012.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  237. IBS-Catalyzed Oxidation of Aromatic Compounds with Oxone

    Tatsuya Mutsuga, Muhammet Uyanik, Kazuaki Ishihara

    92th Annual Spring Meeting of the Chemical Society of Japan 

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    Event date: 2012.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  238. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Kita Spirolactonization of Phenol Derivatives with mCPBA International conference

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    92th Annual Spring Meeting of CSJ 

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    Event date: 2012.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  239. (Hypo)iodite-Catalyzed Oxidative Biaryl Coupling of Phenols with Hydrogen Peroxide International conference

    Dai Nagata, Muhammet Uyanik, Kazuaki Ishihara

    92th Annual Spring Meeting of the Chemical Society of Japan 

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    Event date: 2012.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  240. Chiral (Hypo)iodite-Catalyzed Enantioselective Intramolecular Oxidative Amination to 2-Acylpyrrolidine Derivatives

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    92th Annual Spring Meeting of CSJ 

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    Event date: 2012.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  241. In Situ-Generated (Hypo)iodite-Catalyzed Direct α-Oxyacylation of Carbonyl Compounds with Carboxylic Acids

    Muhammet Uyanik, Daisuke Suzuki, Takeshi Yasui, Kazuaki Ishihara

    The 14th Symposium of the Society of Iodine Science 

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    Event date: 2011.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  242. Chiral (Hypo)iodite Catalyzed Enantioselective Intramolecular Oxidative Etherification to 2-Acylchroman Derivatives

    Hiroki Hayashi, Muhammet Uyanik, Kazuaki Ishihara

    91th Annual Spring Meeting of CSJ 

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    Event date: 2011.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  243. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Kita Spirolactonization with m-CPBA

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    91th Annual Spring Meeting of CSJ 

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    Event date: 2011.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  244. Chiral (Hypo)iodite-Catalyzed Enantioselective Kita Spirolactonization with Hydrogen Peroxide

    Erina Kaneko, Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    91th Annual Spring Meeting of CSJ 

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    Event date: 2011.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  245. Alkali or Alkaline Earth Metal Bulky Borate Salt Catalysis for Baeyer-Villiger Oxidation with Hydrogen Peroxide

    Daisuke Nakashima, Muhammet Uyanik, Kazuaki Ishihara

    91th Annual Spring Meeting of CSJ 

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    Event date: 2011.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  246. (Hypo)Iodite-Catalyzed α-Oxyacylation of Carbonyl Compounds with TBHP

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    91th Annual Spring Meeting of CSJ 

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    Event date: 2011.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  247. Chiral (Hypo)iodite-Catalyzed Enantioselective Intramolecular Oxidative Amination to 2-Acylindoline Derivatives

    Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    91th Annual Spring Meeting of CSJ 

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    Event date: 2011.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  248. Hypervalent Iodine-catalyzed Enantioselective Oxidative Cycloetherification of 3-(2-Hydroxyphenyl)propan-1-ones to 2,3-Dihydrobenzofuran-2-Carbonyl Derivatives International conference

    Kazuaki Ishihara, Muhammet Uyanik, Hiroaki Okamoto, Takeshi Yasui

    The 2010 International Chemical Congress of Pacific Basin Societies (Pacifichem 2010) 

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    Event date: 2010.12

    Language:English   Presentation type:Oral presentation (general)  

    Country:United States  

  249. Quaternary Ammonium (Hypo)iodite Catalysis for Enantioselective Oxidative Cycloetherification

    Muhammet Uyanik, Hiroaki Okamoto, Takeshi Yasui, Kazuaki Ishihara

    The 13th Symposium of the Society of Iodine Science 

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    Event date: 2010.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  250. (Hypo)iodite-Catalyzed a-Oxyacylation of Carbonyl Compounds with TBHP

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    41th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2010.11

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  251. Enviromentally Benign Catalyric Baeyer-Billiger Oxidation with Hydrogen Peroxide

    Daisuke Nakashima, Muhammet Uyanik, Kazuaki Ishihara

    41th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2010.11

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  252. Chiral Hypervalent Iodine-Catalyzed Enantioselective Intramolecular Oxidative Etherification to 2,3-Dihydrobenzofuran-2-Carbonyl Derivatives

    Hiroaki Okamoto, Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    90th Annual Spring Meeting of CSJ 

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    Event date: 2010.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    A ketodihydrobenzofuran is a key skeketone of many biologically active compounds. The efficient synthetic method for those cycloethers is required. We succeeded in chiral hypervalent iodine catalyzed intramolecular oxidative cyclization of the ketophenols to the ketodihydrobenzofurans. Hypervalent iodine is generated in situ from a chiral ammonium iodide and hydrogen peroxide or tert-butyl hydroperoxide as co-oxidant.

  253. Hypervalent Iodine-Catalyzed Oxidative Intermolecular Coupling of Carbonyl Compounds and Carboxylic Acids

    Daisuke Suzuki, Muhammet Uyanik, Kazuaki Ishihara

    90th Annual Spring Meeting of CSJ 

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    Event date: 2010.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    We succeeded in hypervalent iodine catalyzed intermolecular oxidative coupling of ketones and carboxylic acids to the corresponding α-acyloxy ketones in high yield. Hypervalent iodine is generated in situ from quaternary ammonium iodide and tert-butyl hydroperoxide (TBHP) as co-oxidant.

  254. Chiral Hypervalent Iodine(III)-Catalyzed Enantioselective Oxidative Dearomatization of 1-Naphthol Derivatives to Spirolactones

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    90th Annual Spring Meeting of CSJ 

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    Event date: 2010.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    We designed new chiral iodoarenes synthesized from 2,6-dihydroxyiodobenzene and lactate as a chiral source. We acieved highly enantioselcective oxidative dearomatization of 1-naphthol derivatives to spirolactones with chiral hypervalent iodine(III) compounds which prepared in situ from a catalytic amount of chiral iodoarenes in the presence of m-CPBA.

  255. Bromine-Catalyzed Aerobic Oxidation of Alcohols

    Ryota Fukatsu, Muhammet Uyanik, Kazuaki Ishihara

    90th Annual Spring Meeting of CSJ 

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    Event date: 2010.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    We demonstrated that a simple and environmentally benign catalytic system HBr/NaNO2 was very effective for the selective oxidation of alcohols under balloon pressure of O2. Furthermore, the aerobic oxidation of alcohols was also achieved under balloon pressure of air with this HBr/NaNO2/HNO3 catalytic system.

  256. Scale-up of IBS-Catalyzed Oxidation of Alcohols with Oxone andRearrangement-Oxidation of tert-Allylic Alcohols to α,β-Unsaturated Ketones

    Muhammet Uyanik, Ryota Fukatsu, Kazuaki Ishihara

    90th Annual Spring Meeting of CSJ 

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    Event date: 2010.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    We have reported that 2-iodoxybenzenesulfonic acid (IBS) which is in situ, prepared from Oxone and 2-iodobenzenesulfonic acid shows efficient catalytic activity on the alcohol oxidation. Here, we present scale up of the alcohol oxidation. Additionally, we report the IBS-catalyzed rearrangement-oxidation of tert-allylic alcohols to the unsaturated ketones with Oxone.

  257. Hypervalent Iodine-Catalyzed Oxidative Oxylactonization of Ketocarboxylic Acids with Hydrogen Peroxide

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    10th GSC Symposium 

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    Event date: 2010.3

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  258. Hypervalent Iodine-catalyzed Enantioselective Oxidative Cycloetherification of 3-(2-Hydroxyphenyl)propan-1-ones to 2,3-Dihydrobenzofuran-2-carbonyl Derivatives International conference

    Kazuaki Ishihara, Muhammet Uyanik, Hiroaki Okamoto

    The 11th International KYOTO conference 

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    Event date: 2009.11

    Language:English   Presentation type:Oral presentation (general)  

    Country:Japan  

  259. Hypervalent Iodine-Catalyzed Oxidative Rearrangement of Tertiary Allylic Alcohols to Enones with Oxone

    Ryota Fukatsu, Muhammet Uyanik, Kazuaki Ishihara

    40th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2009.11

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  260. Chiral Hypervalent Iodine-Catalyzed Enantioselective Oxidative Cycloetherification of Ketophenols with Hydrogen Peroxide

    Hiroaki Okamoto, Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    40th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2009.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  261. 2-Iodoxybenzenesulfonic Acid (IBS) as an Extremely Active Catalyst for the Oxiadation of Alcohols to Aldehydes, Ketones, and Carboxylic Acids with Oxone International conference

    Kazuaki Ishihara, Muhammet Uyanik

    The International Conference on Green and Sustainable Chemistry 

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    Event date: 2009.8

    Language:English   Presentation type:Oral presentation (general)  

    Country:Singapore  

  262. Chiral Hypervalent Iodine-Catalyzed Enantioselective Oxidative Cycloetherification of Ketophenols with Hydrogen Peroxide

    Hiroaki Okamoto, Muhammet Uyanik, Kazuaki Ishihara

    89th Annual Spring Meeting of CSJ 

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    Event date: 2009.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    We succeeded in hypervalent iodine catalyzed oxidative cyclization of the ketophenols to the ketodihydrobenzofurans. Hypervalent iodine was generated in situ from catalytic amounts of tetraalkylammonium iodide and hydrogen peroxide as co-oxidant. We also succeeded in the enantioselective oxidative cyclization of ketophenols with chiral ammouium iodides.

  263. Hypervalent Iodine(V)-Catalyzed Highly Efficient Oxidation of Alcohols and Its Reaction Mechanism

    Muhammet Uyanik, Matsujiro Akakura, Kazuaki Ishihara

    89th Annual Spring Meeting of CSJ 

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    Event date: 2009.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    We have reported that 2-iodoxybenzenesulfonic acid (IBS) which is in situ prepared from Oxone and 2-iodobenzenesulfonic acid shows more efficient catalytic activity than IBX on the alcohol oxidation. Here, we succeeded in further expanding of the substrate range of the IBS-catalyzed oxidation of alcohols. Additionally, we report the reaction mechanism of the catalytic oxidation.

  264. Chiral Hypervalent Iodine-Catalyzed Oxidative Oxylactonization of Ketocarboxylic Acids with Hydrogen Peroxide

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    89th Annual Spring Meeting of CSJ 

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    Event date: 2009.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    We achieved the oxidative oxylactonization of ketocarboxylic acids to ketolactones with hypervalent iodine compounds which were prepared in situ from catalytic amounts of tetraalkylammonium iodide in the presence of hydrogen peroxide as a terminal oxidant. We also achieved the enantioselective oxylactonization with chiral quaternary ammoniumu iodide.

  265. Hypervalent Iodine(V)-Catalyzed Efficient and Selective Oxidation of Alcohols

    Muhammet Uyanik, Kazuaki Ishihara

    39th Annual Meeting of Union Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2008.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  266. Hypervalent iodine compound-catalyzed oxylactonization of keto carboxylic acids

    Takeshi Yasui, Muhammet Uyanik, Kazuaki Ishihara

    88th Annual Spring Meeting of CSJ 

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    Event date: 2008.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

    Keto lactones are key structures of many natural products and biologically active compounds. The efficient synthetic method for the keto lactones is required. For the first time, we achieved oxylactonization of keto carboxylic acids to keto lactones with hypervalent iodine compounds which were prepared in situ from catalytic amount of iodoarenes and sulfonic acids in presence of stoichiometric oxidants.

  267. Development of Super-IBX Oxidation Catalysis

    Muhammet Uyanik, Kazuaki Ishihara

    88th Annual Spring Meeting of CSJ 

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    Event date: 2008.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  268. Development of Super-IBX Oxidation Catalysis

    Muhammet Uyanik, Kazuaki Ishihara

    8th GSC Symposium 

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    Event date: 2008.3

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  269. "Super IBX"-Catalyzed Oxidatin of Alcohols

    Muhammet Uyanik, Kazuaki Ishihara

    SORST Joint Symposium (8) 

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    Event date: 2008.1

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  270. 2-Iodoxybenzenesulfonic Acid (IBS) as an Extremely Active Catalyst for The Oxidation of Alcohols with Oxone International conference

    Kazuaki Ishihara, Muhammet Uyanik

    International Symposium on Catalysis and Fine Chemicals 2007 

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    Event date: 2007.12

    Language:English   Presentation type:Oral presentation (general)  

    Country:Singapore  

  271. Super IBX Catalyzed Oxidation of Alcohols

    Muhammet Uyanik, Kazuaki Ishihara

    38th Annual Meeting of Union of Chemistry-Related Societies in Chubu Area, Japan 

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    Event date: 2007.11

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  272. Acceleration Effect of IBX-Substituent to Oxidation Catalysis of Alcohols

    Muhammet Uyanik, Kazuaki Ishihara

    87th Annual Spring Meeting of CSJ 

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    Event date: 2007.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  273. Diastereoselective Cyclization of Homo(polyprenyl)arene Analogues Bearing a Terminal Siloxyvinyl Group

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    48th Symposium on The Chemistry of Natural Products 

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    Event date: 2006.10

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  274. Diastereoselective Cyclization of Homo(polyprenyl)arene Analogues Bearing Terminal Siloxyvinyl Group Induced by Acids International conference

    Kazuaki Ishihara, Muhammet Uyanik, Hisashi Yamamoto

    International Conference on Biodiversity and Natural Products (IUPAC, Kyoto, Japan) 

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    Event date: 2006.7

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  275. Stereocontrol on the Catalytic Polyene Cyclization Using a Terminal Siloxyviny Group

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    86th Annual Spring Meeting of CSJ 

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    Event date: 2006.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  276. Stereocontrol on the Catalytic Polyene Cyclization Using a Terminal Siloxyvinyl Group International conference

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    0th International Conference on Cutting Edge Organic Chemistry in Asia (Nagoya, Japan) 

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    Event date: 2006.3

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  277. Stereocontrol on the Catalytic Polyene Cyclization Using a Terminal Siloxyvinyl Group International conference

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    Nagoya University 21st Century COE-HRMS International Conference (Nagoya, Japan) 

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    Event date: 2006.1

    Language:English   Presentation type:Poster presentation  

    Country:Japan  

  278. Biomimetic Synthesis of Caparrapi Oxides, 8-Epicaparrapi Oxides and Dysifrafgin Induced by Artificial Cyclases

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    The 22nd Summer Seminar on Synthetic Organic Chemistry 

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    Event date: 2005.9

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  279. Biomimetic Synthesis of (-)-Caparrapi Oxide and (+)-8-Epicaparrapi Oxide Induced by Artificial Cyclases

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    85th Annual Spring Meeting of CSJ 

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    Event date: 2005.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

  280. Biomimetic Synthesis of (-)-Caparrapi Oxide and (+)-8-Epicaparrapi Oxide Induced by Artificial Cyclases

    Muhammet Uyanik, Kazuaki Ishihara, Hisashi Yamamoto

    Nagoya University 21st Century COE, 2nd Symposium for Young Organic Chemists 

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    Event date: 2004.11

    Language:Japanese   Presentation type:Poster presentation  

    Country:Japan  

  281. The Synthetic Study on Bicyclic Monoterpenoids Using Chiral LBAs

    Muhammet Uyanik, Hideaki Ishibashi, Kazuaki Ishihara, Hisashi Yamamoto

    84th Annual Spring Meeting of CSJ 

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    Event date: 2004.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Country:Japan  

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Other research activities 3

  1. Development of Novel Oxidation Catalyst Systems Using Designer Iodine Catalysis

    2016.1

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    JACI News Letter (No.57)

  2. High-Turnover Hypoiodite Catalysis for Enantioselective Synthesis of Chromans

    2014.7

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    MEXT Innovative Areas "Molecular Activation" News Letter-43

  3. Enantioselective Oxidative Transformations Using Designer Iodine Catalysis

    2011.11

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    Meidai Topics

Research Project for Joint Research, Competitive Funding, etc. 27

  1. Development of High-performance Halogen-based Oxidation Catalysis

    Grant number:21H01932  2021.4 - 2024.3

    Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (B)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  2. Development of Selective Oxidation Reactions Using Iodine Catalysis

    Grant number:18H01973  2018.4 - 2021.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(B)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  3. Design of highly functional catalysts based on acid. base combination chemistry

    Grant number:15H05755  2015.7 - 2020.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(A)

    ISHIHARA Kazuaki

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    Authorship:Collaborating Investigator(s) (not designated on Grant-in-Aid)  Grant type:Competitive

  4. Development of Oxidative Coupling Reactions Using Designer Iodine Catalysis

    Grant number:15H05484  2015.4 - 2018.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Young Scientists(A)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  5. エナンチオ選択的酸化的ポリエン環化反応の開発

    2015.4 - 2017.3

    公益財団法人井上科学振興財団  第7回井上リサーチアヴオード 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  6. Development of Onium (Hypo)iodite Salt-Catalyzed Oxidative Coupling Reactions Using Hydrogen Peroxide or Molecular Oxygen

    Grant number:25105722  2013.4 - 2016.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  7. Oxidative Carbon-Carbon Coupling Reactions Using Organocatalysis

    Grant number:25620078  2013.4 - 2014.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Challenging Exploratory Research

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  8. Hypervalent Iodine-Catalyzed Organic Reactions Directed towards GSC

    Grant number:24245020  2012.4 - 2016.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(A)

    ISHIHARA Kazuaki

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    Authorship:Collaborating Investigator(s) (not designated on Grant-in-Aid)  Grant type:Competitive

  9. Development of Environmentally Benign Selective Oxidation Reactions Using Designer Hypervalent Iodine Catalysts

    Grant number:22750087  2010 - 2012

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Young Scientists(B)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  10. Design of highly functional catalysts based on acid. base combination chemistry

    Grant number:20245022  2008 - 2010

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(A)

    ISHIHARA Kazuaki

      More details

    Authorship:Coinvestigator(s)  Grant type:Competitive

  11. 次亜ヨウ素酸塩触媒を用いるインドール類の酸化的脱芳香族化反応の開発

    2020.4 - 2021.3

    ヨウ素学会  ヨウ素学会 2020年度学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  12. 高活性次亜ハロゲン酸塩触媒を用いる酸化的アジド化反応の開発

    2018.4 - 2019.3

    公益財団法人野口研究所  野口研究所 2017年度野口遵研究助成金 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  13. 次亜ヨウ素酸塩触媒を用いる環境低負荷型不斉酸化的環状エーテル化反応の開発

    2015.4 - 2016.3

    公益財団法人東燃ゼネラル石油研究奨励財団  東燃ゼネラル石油研究奨励財団 第34回研究奨励助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  14. High-Turnover Hypoiodite Catalysis of Enantioselective Oxidative Cycloetherification to Synthesize Optically Active Tocopherols

    2014.7

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  15. Development of Enantioselective Oxidative Cyclization Reactions Directed Toward the Synthesis of Chroman Compounds

    2012.11 - 2013.10

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  16. Development of Enviromentally Benign Oxidative Coupling Reactions Directed Toward the Biaryl Synthesis

    2012.10 - 2013.9

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  17. Development of Environmentally Friendly Synthesis Process for a-Acyloxycarbonyl Compounds

    2011.12 - 2012.7

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  18. 光学活性超原子価ヨウ素触媒を用いるエナンチオ選択的酸化的カップリング反応の開発

    2011.2 - 2012.3

    公益財団法人理工学振興会  理工学振興会 平成23年度研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  19. Development of an Efficient Baeyer-Villiger Oxidation Process Using Hydrogen Peroxide for the Synthesis of e-Caprolactones

    2010.10 - 2011.3

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

  20. 光学活性超原子価ヨウ素触媒を用いるエナンチオ選択的酸化的カップリング反応の開発

    2010.4 - 2011.3

    ヨウ素学会  ヨウ素学会 2010年度学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  21. デザイン型超原子価ヨウ素化合物を触媒に用いる環境低負荷型選択的酸化反応の開発

    2009.4 - 2011.3

    公益財団法人日東学術振興財団  日東学術振興財団 第26回学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  22. デザイン型超原子価ヨウ素化合物を触媒に用いる環境低負荷型選択的酸化反応の開発

    2009.4 - 2011.3

    塩野義製薬株式会社  第21回有機合成化学協会 研究企画賞(塩野義製薬) 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  23. 超原子価ヨウ素を触媒に用いる環境低負荷型選択的酸化反応の開発

    2008.4 - 2009.3

    公益財団法人昭和報公会  昭和報公会 2008年学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  24. 高活性超原子価ヨウ素触媒の設計と選択的酸化反応の開発

    2008.4 - 2009.3

    公益財団法人東燃ゼネラル石油研究奨励財団  東燃ゼネラル石油研究奨励財団 第27回研究奨励助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  25. 超原子価ヨウ素を触媒に用いる環境低負荷型選択的酸化反応の開発

    2007.11 - 2009.12

    名古屋大学  名古屋大学学術振興基金 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  26. 光学活性超原子価ヨウ素触媒の設計及びエナンチオ選択的酸化的ラクトン化反応の開発

    2007.10 - 2008.3

    名古屋大学  名古屋大学グローバルCOEプログラム若手自立的研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  27. 非金属系超原子価ヨウ素化合物を触媒に用いる高効率環境低負荷型アルコール酸化反応の開発と実用的応用

    2007.7 - 2008.3

    科学技術振興機構(JST)地域イノベーション創出総合支援事業「シーズ発掘試験」  JST地域イノベーション創出総合支援事業「シーズ発掘試験」平成19年度公募 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

▼display all

KAKENHI (Grants-in-Aid for Scientific Research) 27

  1. Development of High-performance Halogen-based Oxidation Catalysis

    Grant number:21H01932  2021.4 - 2024.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (B)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

    Grant amount:\17290000 ( Direct Cost: \13300000 、 Indirect Cost:\3990000 )

  2. Development of Selective Oxidation Reactions Using Iodine Catalysis

    Grant number:18H01973  2018.4 - 2021.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(B)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

    Grant amount:\17290000 ( Direct Cost: \13300000 、 Indirect Cost:\3990000 )

  3. Design of highly functional catalysts based on acid. base combination chemistry

    Grant number:15H05755  2015.7 - 2020.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(A)

    ISHIHARA Kazuaki

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    Authorship:Collaborating Investigator(s) (not designated on Grant-in-Aid)  Grant type:Competitive

  4. Development of Oxidative Coupling Reactions Using Designer Iodine Catalysis

    Grant number:15H05484  2015.4 - 2018.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Young Scientists(A)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

    Grant amount:\24180000 ( Direct Cost: \18600000 、 Indirect Cost:\5580000 )

    Although a great advancement has been made in the development of acid-base organocatalysis in recent years, organocatalyzed redox reactions have less investigated. We interested in the redox ability (hypervalent ability) of iodine as an alternative to heavy metals and transition metals. We developed several redox organocatalysis for the highly efficient and selective oxidative transformations based on iodine chemistry. Importantly, the catalytic active species could be generated in situ from the corresponding stable and safe precursors (iodoarenes or onium iodides) in the presence of appropriate oxidants under environmentally friendly conditions.

  5. エナンチオ選択的酸化的ポリエン環化反応の開発

    2015.4 - 2017.3

    公益財団法人井上科学振興財団  第7回井上リサーチアヴオード 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  6. Development of Onium (Hypo)iodite Salt-Catalyzed Oxidative Coupling Reactions Using Hydrogen Peroxide or Molecular Oxygen

    Grant number:25105722  2013.4 - 2016.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

    Grant amount:\6240000 ( Direct Cost: \4800000 、 Indirect Cost:\1440000 )

  7. Oxidative Carbon-Carbon Coupling Reactions Using Organocatalysis

    Grant number:25620078  2013.4 - 2014.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Challenging Exploratory Research

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

    Grant amount:\4030000 ( Direct Cost: \3100000 、 Indirect Cost:\930000 )

    Biaryl compounds and arylquinones are key skeletons of many biologically active compounds and functional organic materials. The efficient and environmentally benign synthetic method for those compounds is required. We succeeded in oxidative biaryl coupling reaction of substituted phenols or naphthols catalyzed by hypoiodite salts, which were generated in situ from the corresponding iodide and aqueous hydrogen peroxide as a co-oxidant. The corresponding biphenols or binaphthols were obtained in moderate to high yields. Additionally, depending on the substrates, diphenoquinones or dinaphthoquinones were also obtained by further oxidations. Moreover, we succeeded in hypoiodite-catalyzed oxidation of hydroquinones to quinones with aqueous hydrogen peroxide. The subsequent one-pot cross coupling of these quinones with aryl compounds could be achieved catalyzed by alkali or alkaline earth metal bulky borate salts to give the corresponding arylquinones in good yields.

  8. Hypervalent Iodine-Catalyzed Organic Reactions Directed towards GSC

    Grant number:24245020  2012.4 - 2016.3

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(A)

    Ishihara Kazuaki

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    Authorship:Collaborating Investigator(s) (not designated on Grant-in-Aid)  Grant type:Competitive

    Hypervalent iodine compounds are very attractive as alternative resources for heavy metal oxidants green & sustainable chemistry. However, iodine is also a rare element resource in halogen elements. Therefore, the catalytic use of iodine sources are much better from a standpoint of element strategy. Thus, we developed several designer iodine catalysts for selective oxidative reactions: (1) chiral quaternary ammonium hypoiodide-catalyzed enantioselective dehydogenative coupling reactions to provide O, and N-heterocycles, (2) chiral iodosoarene-catalyzed enantioselective dearomatizations ti provide spirocyclic sompounds, (3) IBS-catalyzed regioselective oxidation of 2-substituted phenols to 1,2-qinols. In particular, 2-silylmethyl substituent of phenols are effecyive for IBS-catalyzed regioselective oxidation.

  9. Development of Environmentally Benign Selective Oxidation Reactions Using Designer Hypervalent Iodine Catalysts

    Grant number:22750087  2010 - 2012

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Young Scientists(B)

    UYANIK Muhammet

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    Authorship:Principal investigator  Grant type:Competitive

    Grant amount:\4160000 ( Direct Cost: \3200000 、 Indirect Cost:\960000 )

    In this study, we achieved several oxidation reactions using designer hypervalent iodine catalysts. We have developed the first example of the organoiodine(V)-catalyzed regioselective oxidation of phenols to ortho-quinones using 2-iodoxybenzenesulfonic acid (IBS). Moreover, we succeeded in the rational design of conformationally flexible iodosylarenes based on secondary nonbonding interactions as chiral catalysts for the enantioselective oxidative dearomatization of 1-naphthols. Furthermore, we have developed the intra- and intermolecular direct x-oxyacylation reactions of carbonyl compounds catalyzed by in situ-generated ammonium (hypo)iodite species with hydrogen peroxide or TBHP as an environmentally benign oxidant

  10. Design of highly functional catalysts based on acid. base combination chemistry

    Grant number:20245022  2008 - 2010

    Japan Society for the Promotion of Science  Grant-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research(A)

    ISHIHARA Kazuaki

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    Authorship:Coinvestigator(s)  Grant type:Competitive

    Rational design of catalysts is very important to control not only reactivity of target reactions but also chemoselectivity, stereoselectivity, regioselectivity, enantioselectivity, and substrate selectivity. Enzymes almost perfectly control target reactions even in vivo. On the other hand, small molecule artificial catalysts cannot perfectly control reactions. In this research project, the development of new acid. base combined catalysts was performed to attain high level of catalytic functions. As results, we succeeded in the development of several high functional catalysts based on acid. base combination chemistry.

  11. 次亜ヨウ素酸塩触媒を用いるインドール類の酸化的脱芳香族化反応の開発

    2020.4 - 2021.3

    ヨウ素学会  ヨウ素学会 2020年度学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  12. 高活性次亜ハロゲン酸塩触媒を用いる酸化的アジド化反応の開発

    2018.4 - 2019.3

    公益財団法人野口研究所  野口研究所 2017年度野口遵研究助成金 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  13. 次亜ヨウ素酸塩触媒を用いる環境低負荷型不斉酸化的環状エーテル化反応の開発

    2015.4 - 2016.3

    公益財団法人東燃ゼネラル石油研究奨励財団  東燃ゼネラル石油研究奨励財団 第34回研究奨励助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  14. 高活性キラル次亜ヨウ素酸塩触媒を用いるエナンチオ選択的酸化的環状エーテル化反応によるトコフェロールの不斉合成

    2014.7

    公益財団法人 矢崎科学技術振興記念財団  矢崎科学技術振興記念財団 H26年度前期国際交流援助 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  15. クロマン系生理活性物質の環境低負荷型不斉合成法の開発

    2012.11 - 2013.10

    科学技術振興機構(JST)  JST研究成果展開事業(A-STEP)【フィージビリティスタディ(探索タイプ)】平成24年度第2回公募 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  16. 環境調和型酸化的カップリング反応によるビアリール化合物の合成法の開発

    2012.10 - 2013.9

    科学技術振興機構(JST)  JST復興促進プログラム(A-STEP)【フィージビリティスタディ(探索タイプ)】平成24年度公募 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  17. α-アシロキシカルボニル化合物の環境調和型製造法の開発

    2011.12 - 2012.7

    科学技術振興機構(JST)  JST研究成果展開事業(A-STEP)【フィージビリティスタディ(探索タイプ)】平成23年度第2回公募 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  18. 光学活性超原子価ヨウ素触媒を用いるエナンチオ選択的酸化的カップリング反応の開発

    2011.2 - 2012.3

    公益財団法人理工学振興会  理工学振興会 平成23年度研究助成 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  19. 過酸化水素水を酸化剤に用いる触媒的バイヤー・ビリガー酸化反応:ε-カプロラクトンの高効率合成

    2010.10 - 2011.3

    科学技術振興機構(JST)  JST研究成果展開事業(A-STEP)【フィージビリティスタディ(探索タイプ)】平成22年度公募 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

  20. 光学活性超原子価ヨウ素触媒を用いるエナンチオ選択的酸化的カップリング反応の開発

    2010.4 - 2011.3

    ヨウ素学会  ヨウ素学会 2010年度学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  21. デザイン型超原子価ヨウ素化合物を触媒に用いる環境低負荷型選択的酸化反応の開発

    2009.4 - 2011.3

    公益財団法人日東学術振興財団  日東学術振興財団 第26回学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  22. デザイン型超原子価ヨウ素化合物を触媒に用いる環境低負荷型選択的酸化反応の開発

    2009.4 - 2011.3

    塩野義製薬株式会社  第21回有機合成化学協会 研究企画賞(塩野義製薬) 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  23. 超原子価ヨウ素を触媒に用いる環境低負荷型選択的酸化反応の開発

    2008.4 - 2009.3

    公益財団法人昭和報公会  昭和報公会 2008年学術研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  24. 高活性超原子価ヨウ素触媒の設計と選択的酸化反応の開発

    2008.4 - 2009.3

    公益財団法人東燃ゼネラル石油研究奨励財団  東燃ゼネラル石油研究奨励財団 第27回研究奨励助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  25. 超原子価ヨウ素を触媒に用いる環境低負荷型選択的酸化反応の開発

    2007.11 - 2009.12

    名古屋大学  名古屋大学学術振興基金 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  26. 光学活性超原子価ヨウ素触媒の設計及びエナンチオ選択的酸化的ラクトン化反応の開発

    2007.10 - 2008.3

    名古屋大学  名古屋大学グローバルCOEプログラム若手自立的研究助成 

    ウヤヌク ムハメット

      More details

    Authorship:Principal investigator  Grant type:Competitive

  27. 非金属系超原子価ヨウ素化合物を触媒に用いる高効率環境低負荷型アルコール酸化反応の開発と実用的応用

    2007.7 - 2008.3

    科学技術振興機構(JST)地域イノベーション創出総合支援事業「シーズ発掘試験」  JST地域イノベーション創出総合支援事業「シーズ発掘試験」平成19年度公募 

    ウヤヌク ムハメット

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    Authorship:Principal investigator  Grant type:Competitive

▼display all

Industrial property rights 29

  1. New Alkylcarbonyl Lactone Comppund and Method for Producing The Same

    Kazuaki Ishihara, Muhammet Uyanik, Kikuo Furukawa, Hiroyasu Tanaka

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    Applicant:Mitsubishi Gas Chemical Company Inc.; National University Corporation Nagoya University

    Application no:特願2014-204756  Date applied:2014.10

    Announcement no:特開2016-74614  Date announced:2016.5

    Patent/Registration no:特許第6404666号  Date registered:2018.9  Date issued:2018.10

    Rights holder:Mitsubishi Gas Chemical Company Inc.; National University Corporation Nagoya University   Country of applicant:Domestic   Country of acquisition:Domestic

  2. Method for producing optically active aromatic compounds having ring structure that includes nitrogen atom

    Kazuaki Ishihara, Muhammet Uyanik, Daisuke Suzuki

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    Applicant:National University Corporation Nagoya University

    Application no:特願2013-123423  Date applied:2013.6

    Announcement no:特開2014-240365  Date announced:2014.12

    Patent/Registration no:特許第6115946号  Date registered:2017.3  Date issued:2017.4

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic   Country of acquisition:Domestic

  3. Method for producing optically active 2-acylchroman compound and precatalyst used for the same

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2012-194893  Date applied:2012.9

    Announcement no:特開2014-51437  Date announced:2014.3

    Patent/Registration no:特許第6004330号  Date registered:2016.9  Date issued:2016.10

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic   Country of acquisition:Domestic

  4. Iodoarene derivative, method for producing optically active spirolactone compound using same, and method for producing optically active cyclization adduct

    Kazuaki Ishihara, Muhammet Uyanik, Takeshi Yasui

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    Applicant:National University Corporation Nagoya University

    Application no:EP-12754890  Date applied:2012.3

    Announcement no:EP-2684863(A1)  Date announced:2014.1

    Patent/Registration no:EP-2684863(B1)  Date registered:2017.5 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country   Country of acquisition:Foreign country

  5. Iodoarene derivative, method for manufacturing optically active spirolactone compound by using the same, and method for manufacturing optically active cycloadduct

    Kazuaki Ishihara, Muhammet Uyanik, Takeshi Yasui

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    Applicant:National University Corporation Nagoya University

    Application no:US-14/002574  Date applied:2012.3

    Announcement no:US-2013/0338364(A1)  Date announced:2013.12

    Patent/Registration no:US-9000216(B2)  Date registered:2015.4 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2012/121248(A1), 2012.09.13.
    PCT Application: PCT/JP2012/055679, 2012.03.06.
    Application Priority Data: JP2011-052572, 2011.03.10.

  6. Iodoarene derivative, method for producing optically active spirolactone compound using same, and method for producing optically active cyclization adduct

    Kazuaki Ishihara, Muhammet Uyanik, Takeshi Yasui

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    Applicant:National University Corporation Nagoya University

    Application no:特願2013-503554  Date applied:2012.3

    Announcement no:WO2012/121248  Date announced:2012.9

    Publication no:JP/WO2012/121248(A1)  Date published:2014.7

    Patent/Registration no:特許第5688647号  Date registered:2015.2 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic , International (PCT) application   Country of acquisition:Domestic

  7. Method for producing aromatic compound having ring structure that includes nitrogen atom or oxygen atom

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:US-13/982424  Date applied:2012.2

    Announcement no:US-2013/0338371(A1)  Date announced:2013.12

    Patent/Registration no:US-9018394(B2)  Date registered:2015.4 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2012/111449(A1), 2012.08.23.
    PCT Application: PCT/JP2012/052424, 2012.02.02.
    Application Priority Data: JP2011-033808, 2011.02.18.

  8. Method for producing aromatic compound having ring structure that includes nitrogen atom or oxygen atom

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2012-557880  Date applied:2012.2

    Announcement no:WO2012/111449(A1)  Date announced:2012.8

    Publication no:JP/WO2012/111449(A1)  Date published:2014.7

    Patent/Registration no:特許第5929767号  Date registered:2016.5 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic , International (PCT) application   Country of acquisition:Domestic

  9. Method for producing esters

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:EP-11837836  Date applied:2011.10

    Announcement no:EP-2636665(A1)  Date announced:2013.9

    Patent/Registration no:EP-2636665(B1)  Date registered:2016.6 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2012/060185(A1), 2012.05.10.
    PCT Application: PCT/JP2011/073340, 2011.10.11.
    Application Priority Data: JP2010-245944, 2010.11.02.

  10. Method for manufacturing ester

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:US-13/881544  Date applied:2011.10

    Announcement no:US-2013/0217898(A1)  Date announced:2013.8

    Patent/Registration no:US-8853426(B2)  Date registered:2014.10 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2012/060185(A1), 2012.05.10.
    PCT Application: PCT/JP2011/073340, 2011.10.11.
    Application Priority Data: JP2010-245944, 2010.11.02.

  11. Method for producing esters

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2012-541793  Date applied:2011.10

    Announcement no:WO2012/060185(A1)  Date announced:2012.5

    Publication no:JP/WO2012/060185(A1)  Date published:2014.5

    Patent/Registration no:特許第5920889号  Date registered:2016.4 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic , International (PCT) application   Country of acquisition:Domestic

  12. Method for producing α-acyloxycarbonyl compound and novel α-acyloxycarbonyl compound (CN)

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.

    Application no:CN-201410078904  Date applied:2011.3

    Announcement no:CN-103864608(A)  Date announced:2014.6

    Patent/Registration no:CN-103864608(B)  Date registered:2016.3 

    Rights holder:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2011/108696(A1), 2011.09.09.
    PCT Application: PCT/JP2011/055043, 2011.03.04.
    Application Priority Data: JP2010-049003, 2010.03.05.

  13. Method for producing α-acyloxycarbonyl compound and novel α-acyloxycarbonyl compound

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.

    Application no:EP-11750805  Date applied:2011.3

    Announcement no:EP-2543658(A1)  Date announced:2013.1

    Patent/Registration no:EP-2543658(B1)  Date registered:2015.5 

    Rights holder:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2011/108696(A1), 2011.09.09.
    PCT Application: PCT/JP2011/055043, 2011.03.04.
    Application Priority Data: JP2010-049003, 2010.03.05.

  14. Method for producing α-acyloxycarbonyl compound and novel α-acyloxycarbonyl compound (KR)

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.

    Application no:KR-20127023122  Date applied:2011.3

    Announcement no:KR-20130004282(A)  Date announced:2013.1

    Patent/Registration no:KR-101792298(B1)  Date registered:2017.10 

    Rights holder:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2011/108696(A1), 2011.09.09.
    PCT Application: PCT/JP2011/055043, 2011.03.04.
    Application Priority Data: JP2010-049003, 2010.03.05.

  15. Method for producing α-acyloxycarbonyl compound and novel α-acyloxycarbonyl compound

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.

    Application no:US-13/581734  Date applied:2011.3

    Announcement no:US-2012/0323014(A1)  Date announced:2012.12

    Patent/Registration no:US-8680322(B2)  Date registered:2014.3 

    Rights holder:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2011/108696(A1), 2011.09.09.
    PCT Application: PCT/JP2011/055043, 2011.03.04.
    Application Priority Data: JP2010-049003, 2010.03.05.

  16. Method for producing α-acyloxycarbonyl compound (CN)

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.

    Application no:CN-201180012595  Date applied:2011.3

    Announcement no:CN-102834368(A)  Date announced:2012.12

    Patent/Registration no:CN-102834368(B)  Date registered:2015.4 

    Rights holder:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2011/108696(A1), 2011.09.09.
    PCT Application: PCT/JP2011/055043, 2011.03.04.
    Application Priority Data: JP2010-049003, 2010.03.05.

  17. Method for producing α-acyloxycarbonyl compound and novel α-acyloxycarbonyl compound (TW)

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.

    Application no:TW-100107298  Date applied:2011.3

    Announcement no:TW-201139360(A1)  Date announced:2011.11

    Patent/Registration no:TW-I516473(B)  Date registered:2016.1 

    Rights holder:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2011/108696(A1), 2011.09.09.
    PCT Application: PCT/JP2011/055043, 2011.03.04.
    Application Priority Data: JP2010-049003, 2010.03.05.

  18. Method for producing α-acyloxycarbonyl compound and novel α-acyloxycarbonyl compound

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.

    Application no:特願2012-503280  Date applied:2011.3

    Announcement no:WO2011/108696  Date announced:2011.9

    Publication no:JP/WO2011/108696  Date published:2013.6

    Patent/Registration no:特許第5770160号  Date registered:2015.7 

    Rights holder:National University Corporation Nagoya University, Mitsubishi Rayon Co., Ltd.   Country of applicant:Domestic , International (PCT) application   Country of acquisition:Domestic

  19. Iodobenzene derivative and process for preparation of optically active spirolactone compound using same

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2011-538342  Date applied:2010.10

    Announcement no:WO2011/052388(A1)  Date announced:2011.5

    Publication no:JP/WO2011/052388(A1)  Date published:2013.3

    Patent/Registration no:特許第5747332号  Date registered:2015.5 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic , International (PCT) application   Country of acquisition:Domestic

  20. Method for producing carbonyl compound and pro-oxidant used for production of carbonyl compound

    Kazuaki Ishihara, Muhammet Uyanik, Yukihiro Isogai, Suguru Ohara

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    Applicant:National University Corporation Nagoya University

    Application no:特願2009-284483  Date applied:2009.12

    Announcement no:特開2010-100636  Date announced:2010.5

    Patent/Registration no:特許第4590514号  Date registered:2010.9 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic , International (PCT) application   Country of acquisition:Domestic

  21. Method for producing optically active cyclic ether compound and catalyst used for the same

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2009-211609  Date applied:2009.9

    Announcement no:特開2011-057648  Date announced:2011.3

    Patent/Registration no:特許第5544596号  Date registered:2014.5 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Domestic   Country of acquisition:Domestic

  22. Process for preparation of carbonyl compound and pro-oxidant for preparation of carbonyl compound

    Ishihara Kazuaki, Uyanik Muhammet, Isogai Yukihiro, Ohara Suguru

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    Applicant:National University Corporation Nagoya University

    Application no:US-12/441194  Date applied:2008.8

    Announcement no:US-2010/0041917(A1)  Date announced:2010.2

    Patent/Registration no:US-8394995(B2)  Date registered:2013.3 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2009/028676(A1), 2009.03.05
    PCT Application: PCT/JP2008/065567, 2008.08.29.
    Application Priority Data: JP2007-226843, 2007.08.31.

  23. Method for producing carbonyl compound and pro-oxidant used for production of carbonyl compound (CN)

    Kazuaki Ishihara, Muhammet Uyanik, Yukihiro Isogai, Suguru Ohara

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    Applicant:National University Corporation Nagoya University

    Application no:CN-200880000718  Date applied:2008.8

    Announcement no:CN-101541725(A)  Date announced:2009.9

    Patent/Registration no:CN-101541725(B)  Date registered:2013.8 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2009/028676(A1), 2009.03.05
    PCT Application: PCT/JP2008/065567, 2008.08.29.
    Application Priority Data: JP2007-226843, 2007.08.31.

  24. Method for producing carbonyl compound and pro-oxidant used for production of carbonyl compound

    Kazuaki Ishihara, Muhammet Uyanik, Yukihiro Isogai, Suguru Ohara

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    Applicant:National University Corporation Nagoya University

    Application no:EP-08828094  Date applied:2008.8

    Announcement no:EP-2085373(A1)  Date announced:2009.8

    Publication no:EP-2085373(A1) 

    Patent/Registration no:EP-2085373(B1)  Date registered:2013.1 

    Rights holder:National University Corporation Nagoya University   Country of applicant:Foreign country , International (PCT) application   Country of acquisition:Foreign country

    PCT Publication: WO2009/028676(A1), 2009.03.05
    PCT Application: PCT/JP2008/065567, 2008.08.29.
    Application Priority Data: JP2007-226843, 2007.08.31.

  25. Method for producing aryl hydroquinone derivative and aryl quinone derivative

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2014-046259  Date applied:2014.3

    Announcement no:特開2015-168660  Date announced:2015.9

    Country of applicant:Domestic  

  26. Production method for nitrogen-containing cyclic compound, and nitrogen-containing cyclic compound

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2014-500160  Date applied:2013.1

    Announcement no:WO2013/121879(A1)  Date announced:2013.8

    Publication no:JP/WO2013/121879(A1)  Date published:2015.5

    Country of applicant:Domestic , International (PCT) application  

  27. Production method for biaryl compound

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2014-500157  Date applied:2013.1

    Announcement no:WO2013/121873(A1)  Date announced:2013.8

    Publication no:JP/WO2013/121873(A1)  Date published:2015.5

    Country of applicant:Foreign country , International (PCT) application  

  28. Iodoarene derivative, method for producing optically active spirolactone compound using same, and method for producing optically active cyclization adduct (CN)

    Kazuaki Ishihara, Muhammet Uyanik, Takeshi Yasui

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    Applicant:National University Corporation Nagoya University

    Application no:CN-201280012292  Date applied:2012.3

    Announcement no:CN-103415501(A)  Date announced:2013.11

    Country of applicant:Foreign country , International (PCT) application  

    PCT Publication: WO2012/121248(A1), 2012.09.13.
    PCT Application: PCT/JP2012/055679, 2012.03.06.
    Application Priority Data: JP2011-052572, 2011.03.10.

  29. Method for producing carbonyl compound

    Kazuaki Ishihara, Muhammet Uyanik

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    Applicant:National University Corporation Nagoya University

    Application no:特願2007-094377  Date applied:2007.3

    Announcement no:特開2008-247872 

    Country of applicant:Domestic  

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Teaching Experience (On-campus) 72

  1. Advanced Experiments and Exercises in Molecular Chemistry II

    2021

  2. Advanced Experiments and Exercises in Molecular Chemistry I

    2021

  3. Seminar on Molecular Chemistry 1C

    2021

  4. Seminar on Molecular Chemistry 1A

    2021

  5. Fundamentals of Moleuclar and Macromolecular Chemistry

    2021

  6. Chemistry and Biotechnology Laboratory 2

    2021

  7. Organic Chemistry Laboratory I

    2021

  8. Seminar on Molecular Chemistry 2E

    2021

  9. Seminar on Molecular Chemistry 2C

    2021

  10. Seminar on Molecular Chemistry 2A

    2021

  11. Chemistry and Biotechnology Laboratory 3

    2021

  12. Organic Chemistry 2 with Exercises

    2021

  13. Biotechnology Laboratory

    2021

  14. Organic Chemistry Laboratory II

    2021

  15. Organic Chemistry I

    2021

  16. Chemistry and Biotechnology Laboratory 3

    2021

  17. Seminar on Molecular Chemistry 2D

    2021

  18. Seminar on Molecular Chemistry 2B

    2021

  19. Catalysis in Organic Synthesis

    2021

  20. Seminar on Molecular Chemistry 1D

    2021

  21. Seminar on Molecular Chemistry 1B

    2021

  22. Organic Chemistry I

    2020

  23. Organic Chemistry 3 with Exercises

    2020

  24. Organic Chemistry 2 with Exercises

    2020

  25. Organic Chemistry II

    2020

  26. 化学生命工学科実験4(有機化学)

    2020

  27. 化学生命工学科実験2(有機化学)

    2020

  28. Catalysis in Organic Synthesis

    2020

  29. 生物機能工学演習

    2020

  30. Chemistry and Biotechnology Laboratory 4 (Organic Chemistry)

    2019

  31. Chemistry and Biotechnology Laboratory 2 (Organic Chemistry)

    2019

  32. Organic Chemistry 3 and Exercise

    2018

  33. Biotechnology Exercises 1

    2018

  34. Biotechnology Laboratory

    2018

  35. Organic Chemistry Laboratory 1

    2018

  36. Biotechnology Exercises 1

    2017

  37. Biotechnology Laboratory

    2017

  38. Organic Chemistry Laboratory 1

    2017

  39. Biotechnology Exercises 1

    2016

  40. Biotechnology Laboratory

    2016

  41. Organic Chemistry Laboratory 1

    2016

  42. Organic Chemistry Laboratory 1

    2015

  43. Biotechnology Laboratory

    2015

  44. Biotechnology Exercises 1

    2015

  45. Biotechnology Exercises 1

    2014

  46. Biotechnology Laboratory

    2014

  47. Organic Chemistry Laboratory 1

    2014

  48. Organic Chemistry Laboratory 1

    2013

  49. Biotechnology Exercises 1

    2013

  50. Biotechnology Laboratory

    2013

  51. Biotechnology Laboratory

    2012

  52. Organic Chemistry Laboratory 1

    2012

  53. Biotechnology Exercises 1

    2012

  54. Organic Chemistry Laboratory 1

    2011

  55. Biotechnology Exercises 1

    2011

  56. Biotechnology PBL

    2011

  57. Biotechnology Laboratory

    2011

  58. Biotechnology PBL

    2010

  59. Biotechnology Laboratory

    2010

  60. Organic Chemistry Laboratory 1

    2010

  61. Biotechnology Exercises 1

    2010

  62. Biotechnology Exercises 1

    2009

  63. Biotechnology PBL

    2009

  64. Biotechnology Laboratory

    2009

  65. Organic Chemistry Laboratory 1

    2009

  66. Biotechnology Laboratory

    2008

  67. Biotechnology Exercises 1

    2008

  68. Biotechnology PBL

    2008

  69. Organic Chemistry Laboratory 1

    2008

  70. Biotechnology PBL

    2007

  71. Organic Chemistry Laboratory 1

    2007

  72. Biotechnology Exercises 1

    2007

▼display all

 

Media Coverage 59

  1. Hypoiodite Catalysis Permits a General Oxidative Azidation of 1,3-Dicarbonyl Compounds Newspaper, magazine

    2020.9

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  2. アジド化合物 効率生成  名古屋大 優れた官能基許容性 Newspaper, magazine

    化学工業日報  3面  2020.7

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    論文 (Angew. Chem. Int. Ed. 2020, 59, 17110) の内容に関する記

  3. Transition Metal-Free Catalytic Approach Towards Selective Transformations of ortho-Quinone Methides Newspaper, magazine

    2020.6

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  4. 名大大学院研究グループ キノンメチド生成に新手法 医薬品や材料開発の鍵に Newspaper, magazine

    毎日新聞  19面  2020.4

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    論文 (Nature Chem. 2020, 12, 353) の内容に関する記事

  5. 名古屋大 不安定な反応中間体 キノンメチドの新規合成法開発 金属不使用で副生成物はアルコールのみ 新薬開発や医農薬品製造に期待 Newspaper, magazine

    科学新聞  4面  2020.4

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    論文 (Nature Chem. 2020, 12, 353) の内容に関する記事

  6. 医薬品の鍵中間体キノンメチド ヨウ素触媒使い生成 名古屋大 Newspaper, magazine

    化学工業日報  3面  2020.3

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    論文 (Nature Chem. 2020, 12, 353) の内容に関する記事

  7. グリーンイノベーション 環境調和の酸化反応実現 名古屋大学大学院工学研究科ウヤヌク ムハメット氏 第4回GSC奨励賞「デザイン型ヨウ素触媒を用いる新酸化触媒システムの開発 Newspaper, magazine

    化学工業日報  3面  2015.6

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    GSC奨励賞受賞の紹介

  8. 第14回GSC賞・第4回GSC奨励賞発表 【GSC奨励賞】名古屋大学UYANIK, Muhammet「デザイン型ヨウ素触媒を用いる新酸化触媒システムの開発 Newspaper, magazine

    化学工業日報  9面  2015.6

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    GSC奨励賞受賞の紹介

  9. Building Up Quarternary Stereocenters of Chromans by Asymmetric Redox Organocatalysis: A New Entry to Vitamin E Newspaper, magazine

    2014.12

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  10. Enantioselective Synthesis of Tocopherols Through Oxidative Cyclization Newspaper, magazine

    2014.10

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  11. 次亜ヨウ素酸塩触媒を用いて天然型ビタミンEを高効率不斉合成 名古屋大グループ成功 Newspaper, magazine

    科学新聞  4面  2014.8

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    論文 (Science 2014, 345, 291) の内容に関する記事

  12. 酸化反応条件で抗酸化物質を効率的につくる Internet

    Chem-Station  Web portal  2014.7

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    論文 (Science 2014, 345, 291) の内容に関する記事

  13. Green’ Route To Chromanols Newspaper, magazine

    2014.7

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  14. ヨウ素触媒でビタミンE 名大院グループ、不斉合成に成功 Newspaper, magazine

    中日新聞  朝刊3面  2014.7

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    論文 (Science 2014, 345, 291) の内容に関する記事

  15. ビタミンE誘導体 環境対応の合成法 名大ヨウ素触媒で収率99% Newspaper, magazine

    化学工業日報  7面  2014.7

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    論文 (Science 2014, 345, 291) の内容に関する記事

  16. ビタミンE合成効率よく安全に 名古屋大学、触媒開発 Newspaper, magazine

    朝日新聞  夕刊8面  2014.7

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    論文 (Science 2014, 345, 291) の内容に関する記事

  17. 名大、高活性のビタミンE成分を高純度で選択合成することに成功 Newspaper, magazine

    日刊工業新聞  23面  2014.7

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    論文 (Science 2014, 345, 291) の内容に関する記事

  18. Creating antioxidants by oxidation catalysis Newspaper, magazine

    2014.7

  19. ヨウ素触媒性能アップ 柔らかい構造に変化 名大院成功 Newspaper, magazine

    中日新聞  朝刊3面  2013.7

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    論文 (Angew. Chem. Int. Ed. 2013, 52, 9215) の内容に関する記事

  20. 名大 ヨウ素系不斉触媒 収率99%の高活性 Newspaper, magazine

    化学工業日報  4面  2013.7

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    論文 (Angew. Chem. Int. Ed. 2013, 52, 9215) の内容に関する記事

  21. Baeyer-Villiger Oxidation and Oxidative Cascade Reactions with Aqueous Hydrogen Peroxide Catalyzed by Lipophilic LiB(C6F5)4] or Ca[B(C6F5)4]2 Internet

    2013.7

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  22. New catalyst for Baeyer-Villiger oxidation reactions Newspaper, magazine

    2012.11

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  23. 有機化合物から樹脂・医薬品原料 触媒使い安全に合成 名大 Newspaper, magazine

    日刊工業新聞  21面  2012.9

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    論文 (Angew. Chem. Int. Ed. 2012, 51, 909) の内容に関する記事

  24. エコな化学反応発見 名大大学院教授ら 原料生成 爆発の危険性なく Newspaper, magazine

    中日新聞  朝刊31面  2012.8

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    論文 (Angew. Chem. Int. Ed. 2012, 51, 909) の内容に関する記事

  25. CPL原料のε-カプロラクトン 安全で高収率合成 名大 触媒で低毒性金属塩 Newspaper, magazine

    化学工業日報  1面  2012.8

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    論文 (Angew. Chem. Int. Ed. 2012, 51, 909) の内容に関する記事

  26. カルボニル化合物のα-アシロキシ化反応 Newspaper, magazine

    TCIトピックス誌  2012.6

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  48. Clean, Green Chiral Reactions–Just Add a Salt Newspaper, magazine

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