Updated on 2026/03/10

写真a

 
KUWANO SATORU
 
Organization
School of Science Assistant Professor
Title
Assistant Professor
External link

Degree

  • 博士(薬学) ( 京都大学 )

Research Interests

  • 有機元素化学

  • 有機反応化学

  • 触媒化学

  • 不斉合成

Research Areas

  • Nanotechnology/Materials / Structural organic chemistry and physical organic chemistry

  • Nanotechnology/Materials / Synthetic organic chemistry

  • Manufacturing Technology (Mechanical Engineering, Electrical and Electronic Engineering, Chemical Engineering) / Catalyst and resource chemical process

Research History

  • Institute of Science Tokyo   Assistant Professor

    2024.10

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  • Tokyo Institute of Technology   School of Science   Assistant Professor

    2020.5 - 2024.9

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  • Chiba University   Graduate School of Science

    2015.11 - 2020.4

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  • Daiichi University, College of Pharmaceutical Sciences   Faculty of Pharmaceutical Sciences   Assistant Professor

    2014.4 - 2015.10

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Professional Memberships

Papers

  • Reusable Selenenyl Iodide-Initiated Cascade Cyclization of Polyenes with N-terminating Groups

    Satoru Kuwano, Jun Kikushima, Takaaki Nakada, Shohei Sase, Kei Goto

    CHEMISTRY-AN ASIAN JOURNAL   20 ( 14 )   2025.7

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

    DOI: 10.1002/asia.202500347

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  • Highly Electrophilic Intermediates in the Bypass Mechanism of Glutathione Peroxidase: Synthesis, Reactivity, and Structures of Selenocysteine-Derived Cyclic Selenenyl Amides Reviewed

    Ryosuke Masuda, Takafumi Karasaki, Shohei Sase, Satoru Kuwano, Kei Goto

    Chemistry - A European Journal   29 ( 71 )   2023.12

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

    DOI: 10.1002/chem.202302615

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  • Remote Electronic Effect of Chiral N-Heterocyclic Carbene Catalyst on an Asymmetric Benzoin Reaction Reviewed

    Tsubasa Inokuma, Kentaro Hashimoto, Tatsuya Fujiwara, Chunzhao Sun, Satoru Kuwano, Ken ichi Yamada

    Chemistry - A European Journal   29 ( 38 )   2023.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/chem.202300858

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  • Modeling Selenoprotein Se-Nitrosation: Synthesis of a Se-Nitrososelenocysteine with Persistent Stability Reviewed

    Ryosuke Masuda, Satoru Kuwano, Kei Goto

    Journal of the American Chemical Society   145 ( 26 )   14184 - 14189   2023.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/jacs.3c03394

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  • Efficient oxyselenation and aminoselenation utilizing a selenenyl iodide based on the characteristic thermodynamics of its reaction with olefins Reviewed

    Satoru Kuwano, Erika Takahashi, Jun Kikushima, Shohei Sase, Kei Goto

    New Journal of Chemistry   47 ( 20 )   9569 - 9574   2023.3

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    Authorship:Lead author   Publishing type:Research paper (scientific journal)   Publisher:Royal Society of Chemistry (RSC)  

    DOI: 10.1039/d2nj06346h

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  • Remote electronic effect on the N-heterocyclic carbene-catalyzed asymmetric intramolecular Stetter reaction and structural revision of products Reviewed

    Tsubasa Inokuma, Kohei Iritani, Yuki Takahara, Chunzhao Sun, Yousuke Yamaoka, Satoru Kuwano, Ken-ichi Yamada

    Chemical Communications   59 ( 36 )   5375 - 5378   2023

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    Publishing type:Research paper (scientific journal)   Publisher:Royal Society of Chemistry (RSC)  

    The remote electron-withdrawing substituents on the chiral N-heterocyclic carbene enhanced rate and enantioselectivity in the asymmetric intramolecular Stetter reaction. The absolute configurations of the products were revised by X-ray diffraction.

    DOI: 10.1039/d3cc00693j

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  • Stable cysteine sulfenic acid: synthesis by direct oxidation of a thiol, crystallographic analysis, and elucidation of reactivities Invited Reviewed

    Kei Goto, Tsukasa Sano, Ryosuke Masuda, Shotaro Otaka, Ryutaro Kimura, Shohei Sase, Satoru Kuwano

    Phosphorus, Sulfur and Silicon and the Related Elements   198 ( 6 )   466 - 470   2023

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1080/10426507.2023.2195650

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  • Kinetic Resolution of α‐Hydroxyamide via N‐Heterocyclic Carbene‐Catalyzed Acylation Reviewed

    Ken‐ichi Yamada, Akiho Yamauchi, Tatsuya Fujiwara, Keiji Hashimoto, Yinli Wang, Satoru Kuwano, Tsubasa Inokuma

    Asian Journal of Organic Chemistry   11 ( 10 )   2022.9

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

    DOI: 10.1002/ajoc.202200452

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    Other Link: https://onlinelibrary.wiley.com/doi/full-xml/10.1002/ajoc.202200452

  • Model Study on the Catalytic Cycle of Glutathione Peroxidase Utilizing Selenocysteine-Containing Tripeptides: Elucidation of the Protective Bypass Mechanism Involving Selenocysteine Selenenic Acids Reviewed

    Ryosuke Masuda, Satoru Kuwano, Shohei Sase, Marco Bortoli, Andrea Madabeni, Laura Orian, Kei Goto

    Bulletin of the Chemical Society of Japan   95 ( 9 )   1360 - 1379   2022.9

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    DOI: 10.1246/bcsj.20220156

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  • Enhanced Molecular Recognition through Substrate–Additive Complex Formation in N-Heterocyclic-Carbene-Catalyzed Kinetic Resolution of α-Hydroxythioamides Reviewed

    Yinli Wang, Akiho Yamauchi, Keiji Hashimoto, Tatsuya Fujiwara, Tsubasa Inokuma, Yuta Mitani, Koichi Ute, Satoru Kuwano, Yousuke Yamaoka, Kiyosei Takasu, Ken-ichi Yamada

    ACS Catalysis   12 ( 10 )   6100 - 6107   2022.5

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

    DOI: 10.1021/acscatal.2c01579

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  • Chiral Aminomethylbinaphthol-Catalyzed Diastereo- and Enantioselective Epoxidation of Trisubstituted Acrylonitriles Reviewed

    Eri Ogino, Satoru Kuwano, Takayoshi Arai

    Advanced Synthesis and Catalysis   364 ( 8 )   1503 - 1506   2022.4

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/adsc.202200036

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  • Oxy- and aminoselenation of alkenes utilizing an isolable selenenyl iodide Reviewed

    Satoru Kuwano, Erika Takahashi, Kazuaki Ebisawa, Yo Ishikawa, Shohei Sase, Kei Goto

    Mendeleev Communications   32 ( 1 )   80 - 82   2022.3

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    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:Elsevier {BV}  

    DOI: 10.1016/j.mencom.2022.01.026

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  • Late-Stage Functionalization of the Periphery of Oligophenylene Dendrimers with Various Arene Units via Fourfold C-H Borylation Reviewed

    Ryosuke Masuda, Satoru Kuwano, Kei Goto

    Journal of Organic Chemistry   86 ( 21 )   14433 - 14443   2021.11

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.joc.1c01252

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  • Enantio- and diastereoselective double Mannich reaction of malononitrile with N-Boc imines using quinine-derived bifunctional organoiodine catalyst. Reviewed International journal

    Satoru Kuwano, Eri Ogino, Takayoshi Arai

    Organic & Biomolecular Chemistry   19 ( 32 )   6969 - 6973   2021.8

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

    A chiral quinine-derived organic base catalyst with halogen bond donor functionality was used to catalyze the asymmetric double Mannich reaction of malononitrile with N-Boc and N-Cbz imines to afford 1,3-diamines in excellent yields with high enantio- and diastereoselectivities. With 2.2 equiv. of a single imine electrophile, symmetrical 1,3-diamines were obtained, whereas, with two different imine partners, unsymmetrically substituted 1,3-diamine was obtained. The monohydration of the double Mannich product was also achieved.

    DOI: 10.1039/d1ob00796c

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  • A Hypervalent Cyclic Dibenzoiodolium Salt as a Halogen-Bond-Donor Catalyst for the [4+2] Cycloaddition of 2-Alkenylindoles. Reviewed International journal

    Yuki Nishida, Takumi Suzuki, Yuri Takagi, Emi Amma, Ryoya Tajima, Satoru Kuwano, Takayoshi Arai

    ChemPlusChem   86 ( 5 )   741 - 744   2021.4

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    A stable, hypervalent cyclic dibenzoiodolium salt acted as a strong halogen bonding (XB)-donor catalyst for [4+2] cycloaddition of 2-alkenylindoles, and not as an oxidizing agent. The cross-[4+2] cycloaddition of 2-vinylindoles with 2-alkenylindoles was catalyzed smoothly by the hypervalent cyclic dibenzoiodolium triflate catalyst to give the tetrahydrocarbazoles in up to 99 % yield with 17 : 1 diastereoselectivity. The hypervalent cyclic dibenzoiodolium salt was also applicable to the Povarov reaction of 2-vinylindole with N-p-methoxyphenyl (PMP) imine to give the indolyl-tetrahydroquinoline in 83 % yield.

    DOI: 10.1002/cplu.202100089

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  • Chiral C2-Symmetric Aminomethylbinaphthol as Synergistic Catalyst for Asymmetric Epoxidation of Alkylidenemalononitriles: Easy Access to Chiral Spirooxindoles. Reviewed International journal

    Eri Ogino, Ayu Nakamura, Satoru Kuwano, Takayoshi Arai

    Organic Letters   23 ( 6 )   1980 - 1985   2021.2

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    Chiral C2-symmetric 3,3'-bis((R,R)-2-naphthylethylaminomethyl)-(R)-binaphthol (AMB4) functions as an efficient organocatalyst for the asymmetric epoxidation of various alkylidenemalononitriles. The spiro-epoxyoxindole products obtained from isatilidenemalononitriles were easily transformed to the corresponding chiral dihydroquinoxalinyl spirooxindoles.

    DOI: 10.1021/acs.orglett.0c04245

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  • Catalytic Asymmetric Chlorination of β-Ketoesters Using N-PFB-PyBidine-Zn(OAc)2 Reviewed

    Ma, J., Suzuki, T., Kuwano, S., Arai, T.

    Catalysts   10 ( 10 )   1177 - 1185   2020.10

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.3390/catal10101177

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  • Chiral Dinuclear Benzyliminobinaphthoxy-Palladium Catalyst for Asymmetric Mannich Reaction of Aldimines and Isatin-Derived Ketimines with Alkylmalononitriles Reviewed

    Nakamura, A., Kuwano, S., Sun, J., Araseki, K., Ogino, E., Arai, T.

    Advanced Synthesis and Catalysis   362 ( 15 )   3105 - 3109   2020.8

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

    DOI: 10.1002/adsc.202000447

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    Other Link: https://onlinelibrary.wiley.com/doi/full-xml/10.1002/adsc.202000447

  • Non-Bonding Electron Pair versus pi-Electrons in Solution Phase Halogen Bond Catalysis: Povarov Reaction of 2-Vinylindoles and Imines Reviewed

    Takumi Suzuki, Satoru Kuwano, Takayoshi Arai

    Advanced Synthesis & Catalysis   362 ( 15 )   3208 - 3212   2020.8

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

    DOI: 10.1002/adsc.202000494

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  • Catalytic Asymmetric Mannich-Type Reaction of Malononitrile with N-Boc alpha-Ketiminoesters Using Chiral Organic Base Catalyst with Halogen Bond Donor Functionality Reviewed

    Satoru Kuwano, Yuki Nishida, Takumi Suzuki, Takayoshi Arai

    Advanced Synthesis & Catalysis   362 ( 8 )   1674 - 1678   2020.4

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

    DOI: 10.1002/adsc.202000092

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  • Chiral Benzazaborole-Catalyzed Regioselective Sulfonylation of Unprotected Carbohydrate Derivatives Reviewed

    Satoru Kuwano, Yusei Hosaka, Takayoshi Arai

    Chemistry – A European Journal   25 ( 56 )   12920 - 12923   2019.10

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

    DOI: 10.1002/chem.201903443

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  • Bis(imidazolidine)pyridine-CoCl2: A Novel, Catalytically Active Neutral Complex for Asymmetric Michael Reaction of 1,3-Carbonyl Compounds with Nitroalkenes Reviewed

    Takayoshi Arai, Yuko Iimori, Mayu Shirasugi, Ryota Shinohara, Yuri Takagi, Takumi Suzuki, Junma Ma, Satoru Kuwano, Hyuma Masu

    Advanced Synthesis & Catalysis   361 ( 16 )   3704 - 3711   2019.8

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

    DOI: 10.1002/adsc.201900421

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  • Catalysis Based on C−I⋅⋅⋅π Halogen Bonds: Electrophilic Activation of 2‐Alkenylindoles by Cationic Halogen‐Bond Donors for [4+2] Cycloadditions

    Satoru Kuwano, Takumi Suzuki, Masahiro Yamanaka, Ryosuke Tsutsumi, Takayoshi Arai

    Angewandte Chemie   131 ( 30 )   10326 - 10330   2019.7

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

    DOI: 10.1002/ange.201904689

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  • Catalysis Based on C-I pi Halogen Bonds: Electrophilic Activation of 2-Alkenylindoles by Cationic Halogen-Bond Donors for [4+2] Cycloadditions Reviewed

    Satoru Kuwano, Takumi Suzuki, Masahiro Yamanaka, Ryosuke Tsutsumi, Takayoshi Arai

    Angewandte Chemie International Edition   58 ( 30 )   10220 - 10224   2019.7

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

    DOI: 10.1002/anie.201904689

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  • Chiral benzazaboroles as catalysts for enantioselective sulfonylation of cis-1,2-diols Reviewed

    Satoru Kuwano, Yusei Hosaka, Takayoshi Arai

    Organic & Biomolecular Chemistry   17 ( 18 )   4475 - 4482   2019.5

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

    DOI: 10.1039/c8ob03205j

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  • 2-IODOIMIDAZOLINIUM SALT-CATALYZED FRIEDEL-CRAFTS REACTION: SYNTHESIS OF BIS(INDOLYL)METHANE ALKALOIDS Reviewed

    Satoru Kuwano, Takumi Suzuki, Takayoshi Arai

    Heterocycles   97 ( 1 )   163 - 169   2018.9

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

    DOI: 10.3987/COM-18-S(T)33

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  • A chiral organic base catalyst with halogen-bonding-donor functionality: asymmetric Mannich reactions of malononitrile with N-Boc aldimines and ketimines Reviewed

    Satoru Kuwano, Takumi Suzuki, Yusei Hosaka, Takayoshi Arai

    Chemical Communications   54 ( 31 )   3847 - 3850   2018.4

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

    DOI: 10.1039/c8cc00865e

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  • Catalytic Asymmetric Mannich Reaction of Isatin-derived N-Boc Imines with Malononitrile by Bis(imidazolidine)-derived Pincer Rh Complex Reviewed

    Takayoshi Arai, Takuya Tosaka, Satoru Kuwano

    ChemistrySelect   2 ( 24 )   7368 - 7371   2017.8

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

    DOI: 10.1002/slct.201701444

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  • Site-selective benzoin-type cyclization of unsymmetrical dialdoses catalyzed by N-heterocyclic carbenes for divergent cyclitol synthesis Reviewed

    Bubwoong Kang, Yinli Wang, Satoru Kuwano, Yousuke Yamaoka, Kiyosei Takasu, Ken-ichi Yamada

    Chemical Communications   53 ( 32 )   4469 - 4472   2017.4

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    DOI: 10.1039/c7cc01191a

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  • N-HETEROCYCLIC CARBENE-PROMOTED [3+2] CYCLOADDITION OF ALLENYL SULFONE AND ARYLIDENEMALONONITRILES Reviewed

    Satoru Kuwano, Toshinobu Masuda, Koki Yamaguchi, Takayoshi Arai

    Heterocycles   95 ( 1 )   232 - 242   2017.1

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

    DOI: 10.3987/COM-16-S(S)8

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  • Chiral Bis(imidazolidine)iodobenzene (I-Bidine) Organocatalyst for Thiochromane Synthesis Using an Asymmetric Michael/Henry Reaction Reviewed

    Takayoshi Arai, Takumi Suzuki, Takahiro Inoue, Satoru Kuwano

    Synlett   28 ( 1 )   122 - 127   2017.1

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

    DOI: 10.1055/s-0036-1588614

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  • Oxa- and Azacycle Formation via Migrative Cyclization of Sulfonylalkynol and Sulfonylalkynamide with N-Heterocyclic Carbene Reviewed

    Yinli Wang, Raphael Oriez, Satoru Kuwano, Yousuke Yamaoka, Kiyosei Takasu, Ken-ichi Yamada

    The Journal of Organic Chemistry   81 ( 6 )   2652 - 2664   2016.3

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    DOI: 10.1021/acs.joc.6b00182

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  • N-Heterocyclic Carbene Catalyzed Monoacylation of Vicinal Diols Reviewed

    Satoru Kuwano, Toshinobu Masuda

    Synthesis   48 ( 4 )   573 - 578   2016.2

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

    DOI: 10.1055/s-0035-1560544

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  • Catalytic asymmetric [3+2]-cycloaddition for stereodivergent synthesis of chiral indolyl-pyrrolidines Reviewed

    Takayoshi Arai, Chihiro Tokumitsu, Tomoya Miyazaki, Satoru Kuwano, Atsuko Awata

    Organic & Biomolecular Chemistry   14 ( 5 )   1831 - 1839   2016

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

    DOI: 10.1039/c5ob02278a

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  • N-Heterocyclic Carbene-Catalyzed Benzoin Strategy for Divergent Synthesis of Cyclitol Derivatives from Alditols Reviewed

    Bubwoong Kang, Toshiaki Sutou, Yinli Wang, Satoru Kuwano, Yousuke Yamaoka, Kiyosei Takasu, Ken-ichi Yamada

    Advanced Synthesis & Catalysis   357 ( 1 )   131 - 147   2015.1

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    DOI: 10.1002/adsc.201400712

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  • Kinetic Resolution of Secondary Alcohols Catalyzed by Chiral Phosphoric Acids Reviewed

    Shingo Harada, Satoru Kuwano, Yousuke Yamaoka, Ken-ichi Yamada, Kiyosei Takasu

    Angewandte Chemie International Edition   52 ( 39 )   10227 - 10230   2013.9

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    DOI: 10.1002/anie.201304281

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  • Enhanced Rate and Selectivity by Carboxylate Salt as a Basic Cocatalyst in Chiral N-Heterocyclic Carbene-Catalyzed Asymmetric Acylation of Secondary Alcohols Reviewed

    Satoru Kuwano, Shingo Harada, Bubwoong Kang, Raphael Oriez, Yousuke Yamaoka, Kiyosei Takasu, Ken-ichi Yamada

    Journal of the American Chemical Society   135 ( 31 )   11485 - 11488   2013.8

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

    DOI: 10.1021/ja4055838

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  • Chemoselective conversion of alpha-unbranched aldehydes to amides, esters, and carboxylic acids by NHC-catalysis Reviewed

    Satoru Kuwano, Shingo Harada, Raphael Oriez, Ken-ichi Yamada

    Chemical Communications   48 ( 1 )   145 - 147   2012

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

    DOI: 10.1039/c1cc15539c

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MISC

  • システインスルフェン酸を捕まえる-化学プローブを用いた高反応性化学種の検出

    鍬野 哲, 後藤 敬

    月刊化学   77 ( 7 )   70 - 71   2022.7

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  • 不活性アルケンの自由自在なジアミノ化反応-ヨウ素触媒とクロラミン塩窒素源を活用-

    鍬野 哲

    月刊化学   77 ( 2 )   60 - 61   2022.2

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  • 速度論的に制御された“E-選択的な”オレフィンメタセシス

    鍬野 哲

    ファルマシア   53 ( 3 )   260 - 260   2017.3

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    Language:Japanese   Publisher:公益社団法人 日本薬学会  

    オレフィンメタセシスは,二種のオレフィンから結合の組み替えが起こり,新たなオレフィンが生成する反応である.一般的に可逆反応であるため,熱力学的に安定な異性体が優先して得られる.1, 2-二置換オレフィンの多くはE体のほうが熱力学的に安定であるが,ハロゲン化アルケニル化合物の場合,Z体のほうが熱力学的に安定である(図1-①).そのため,既存のメタセシス反応によるE-選択的な合成は困難であった.今回,Hoveydaらによって嵩高いアリールオキシ配位子を持つモリブデン錯体触媒を用いて,速度論的制御に基づいたE-選択的なオレフィンメタセシス反応が報告されたので紹介する.<br>なお,本稿は下記の文献に基づいて,その研究成果を紹介するものである.<br>1) Hoveyda A. H., Zhugralin A. R., Nature, 450, 243-251(2007).<br>2) Wiberg K. B. et al., J. Chem. Theory Comput., 5, 1033-1037(2009).<br>3) Nguyen T. T. et al., Science, 352, 569-575(2016).

    DOI: 10.14894/faruawpsj.53.3_260

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Awards

  • 平成29年度有機合成化学協会東レ研究企画賞

    2017.12   公益社団法人有機合成化学協会   多価アルコールの活性化を志向したキラルアリールボロン酸触媒の創製と応用

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  • 平成25年度笹川科学研究奨励賞

    2014.4   公益財団法人日本科学協会   新規多機能型キラルカルベン触媒の開発とその応用

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  • 日本薬学会第133年会(横浜)優秀発表賞

    2013.3  

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Research Projects

  • 生体反応中間体によるπ結合活性化を基盤とする多連続複素環骨格の一挙構築

    Grant number:22K05063  2022.4 - 2025.3

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

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    Authorship:Principal investigator 

    Grant amount:\4290000 ( Direct Cost: \3300000 、 Indirect Cost:\990000 )

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  • ヨウ化セレネニルのヨウ素化による高反応性化学種の発生と応用

    2021.4 - 2022.3

    2021年度ヨウ素研究助成 

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  • Development of straightforward molecular transformation method of unprotected carbohydrates using chiral organoboron catalyst

    Grant number:19K15553  2019.4 - 2021.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Early-Career Scientists

    Kuwano Satoru

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    Authorship:Principal investigator  Grant type:Competitive

    Grant amount:\4290000 ( Direct Cost: \3300000 、 Indirect Cost:\990000 )

    Although multi-step protection/deprotection methods have been used for the synthesis of sugars, in recent years, development of new one-step regioselective functionalization methods for unprotected sugars is required. In this study, we achieved regioselective functionalization of various unprotected sugars such as galactose, galactosamine, arabinose, rhamnose, and mannose in a single step using originally developed chiral organoboron catalysts. Furthermore, utilizing this method, we achieved kinetic resolution of unprotected sugars via regioselective sulfonylation.

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  • ハロゲン結合を基盤としたヨウ素/窒素協働作用型キラル分子性触媒の創製と応用

    2019.4 - 2020.3

    双葉電子記念財団平成31年度自然科学研究助成 

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  • ハロゲン結合ドナー型キラルヨウ素触媒の創製研究

    2017.4 - 2018.3

    2016年度ヨウ素研究助成 

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  • Development of Methodology for Construction of Cyclic Skeletons Using NHC-Catalyzed Umpolung-Type Gamma-Addition Reaction

    Grant number:15K18841  2015.4 - 2018.3

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

    Kuwano Satoru

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    Authorship:Principal investigator  Grant type:Competitive

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

    The cyclic skeleton is a component included in many biologically active compounds, and the development of a novel methodology for construction of cyclic skeletons is an important research topic leading to the creation of medicines, agricultural chemicals and the like. In this research, we aimed to develop a new method for the synthesis of carbocycles using N-heterocyclic carbene (NHC)-catalyzed umpolung-type γ addition reaction. As a result of various investigations, the γ addition reaction promoted by the addition of NHC proceeded and succeeded in the synthesis of the multiply substituted cyclopentene derivative. We also found that various indole derivatives can be synthesized by using halogen bond donating type iodine catalyst induced by iodination of NHC in the process of this investigation.

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  • Enhanced Rate and Selectivity by Carboxylate Salt as a Basic Cocatalyst in Chiral N-Heterocyclic Carbene-Catalyzed Asymmetric Acylation of Secondary Alcohols

    2013.9 - 2013.12

    平成25年度第2期吉田科学技術財団国際研究集会派遣研究者助成 

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