中村 正治

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Name(Kanji/Kana/Abecedarium Latinum)
中村 正治/ナカムラ マサハル/Nakamura, Masaharu
Primary Affiliation(Org1/Job title)
Institute for Chemical Research (ICR)/Professor
Affiliated programs (koza)
Org1 Job title
Graduate Schools Engineering Professor
Contact Address
Type Address(Japanese) Address(English)
Office 京都府宇治市五ケ庄官有地 Gokasho, Uji, Kyoto, 611-0011, Japan
E-mail Address
E-mail address
masaharu ＠ scl.kyoto-u.ac.jp
masaharu.mac ＠ me.com
Academic Organizations You are Affiliated to in Japan
Organization name(Japanese) Organization name(English)
日本化学会 The Chemical Society of Japan
有機合成化学協会 The Society of Synthetic Organic Chemistry, Japan
近畿化学協会 The Kinki Chemical Society Japan
触媒学会 Catalysis Society of Japan
Academic Degree
Field(Japanese) Field(English) University(Japanese) University(English) Method
博士（理学） D. Sc. 東京工業大学 Tokyo Institute of Technology
Graduate School
University(Japanese) University(English) Faculty(Japanese) Faculty(English) Major(Japanese) Major(English) Degree
東京工業大学 Tokyo Institute of Technology 大学院理工学研究科化学専攻修士課程 Graduate School of Science and Technology Department of Chemistry 修了
東京工業大学 Tokyo Institute of Technology 大学院理工学研究科化学専攻博士課程 Graduate School of Science and Technology Department of Chemistry 修了
Undergraduate School / Major(s)
University(Japanese) University(English) Faculty(Japanese) Faculty(English) Major(s)(Japanese) Major(s)(English) Degree
東京理科大学 Tokyo University of Science 理学部第一部応用化学科 Faculty of Science Department of Applied Chemistry 卒業
High School
Highschool Kana
東京都立西高等学校 とうきょうとりつにしこうとうがっこう
Work Experience
Period Organization(Japanese) Organization(English) Job title(Japanese) Job title(English)
1996/04/-2002/02/ 東京大学大学院理学系研究科化学専攻化学科 Department of Chemistry, The University of Tokyo 助手 assistant professor
2002/03/-2004/02/ 東京大学大学院理学系研究科化学専攻化学科 Department of Chemistry, The University of Tokyo 講師 lecturer
2004/03/-2005/12/ 東京大学大学院理学系研究科化学専攻化学科 Department of Chemistry, The University of Tokyo 助教授 associate professor
2006/01/- 京都大学化学研究所附属元素科学国際研究センター International Research Center for Elements Science, Institute for Chemical Research, Kyoto University 教授 professor
Language of Instruction
Language(japanese) Language(english) Code
英語
Personal Website(s) (URL(s))
URL
http://es.kuicr.kyoto-u.ac.jp/
ORCID ID
https://orcid.org/0000-0002-1419-2117
researchmap URL
https://researchmap.jp/read0206994
Research Topics
(Japanese)
次世代有機合成化学の開拓（炭素資源・金属資源の活用，機能性有機分子の創製と効率合成）有機分子変換科学・元素科学に基づく有機反応化学・超分子触媒の創製と精密有機合成への応用
(English)
synthetic molecular transformation, organic reaction chemistry, synthetic methodology toward exploitation of chemical resources, supramolecular metal catalyst
Overview of the research
(Japanese)
新たな機能や反応性を持つ有機金属化合物による次世代合成化学の開拓」を目標に、人類の未来を支えるような新反応や新物質を創り出すべく，有機合成化学の最先端課題を設定し，取り組んでいます。
(English)
"Exploitation of the new generation chemistry by developing unvailed function and reactivity of organometallics" Our research is directed toward discovering new reactions and functional molecules and developing sustainable chemical resources to change our society for the better.
Fields of research (key words)
Key words(Japanese) Key words(English)
有機合成化学 synthetic organic chemistry
化学合成 chemical syntheis
分子変換 molecular transformation
触媒 catalysis
化学資源 chemical resources
Published Papers
Author Author(Japanese) Author(English) Title Title(Japanese) Title(English) Bibliography Bibliography(Japanese) Bibliography(English) Publication date Refereed paper Language Publishing type Disclose
Iwamoto, T, Okuzono, C, Adak, L, Jin, M, Nakamura, M Iwamoto, T, Okuzono, C, Adak, L, Jin, M, Nakamura, M Iwamoto, T, Okuzono, C, Adak, L, Jin, M, Nakamura, M Iron-Catalysed Enantioselective Suzuki–Miyaura Coupling of Racemic Alkyl Bromides Iron-Catalysed Enantioselective Suzuki–Miyaura Coupling of Racemic Alkyl Bromides Iron-Catalysed Enantioselective Suzuki–Miyaura Coupling of Racemic Alkyl Bromides Chem. Commun., 55, 1128-1131 Chem. Commun., 55, 1128-1131 Chem. Commun., 55, 1128-1131 2019 Refereed English Disclose to all
Agata, R, Kawamura, S, Isozaki, K, Nakamura, M Agata, R, Kawamura, S, Isozaki, K, Nakamura, M Agata, R, Kawamura, S, Isozaki, K, Nakamura, M Iron-catalyzed Alkyl–Alkyl Negishi Coupling of Organoaluminum Reagents Iron-catalyzed Alkyl–Alkyl Negishi Coupling of Organoaluminum Reagents Iron-catalyzed Alkyl–Alkyl Negishi Coupling of Organoaluminum Reagents Chem. Lett., 48, 238-241 Chem. Lett., 48, 238-241 Chem. Lett., 48, 238-241 2019 Refereed English Disclose to all
Agata, R, Takaya, H, Matsuda, H, Nakatani, N, Takeuchi, K, Iwamoto, T, Hatakeyama, T, Nakamura, M Agata, R, Takaya, H, Matsuda, H, Nakatani, N, Takeuchi, K, Iwamoto, T, Hatakeyama, T, Nakamura, M Agata, R, Takaya, H, Matsuda, H, Nakatani, N, Takeuchi, K, Iwamoto, T, Hatakeyama, T, Nakamura, M Iron-Catalyzed Cross Coupling of Aryl Chlorides with Alkyl Grignard Reagents: Synthetic Scope and FeII/FeIV Mechanism Supported by X-ray Absorption Spectroscopy and Density Functional Theory Calculations Iron-Catalyzed Cross Coupling of Aryl Chlorides with Alkyl Grignard Reagents: Synthetic Scope and FeII/FeIV Mechanism Supported by X-ray Absorption Spectroscopy and Density Functional Theory Calculations Iron-Catalyzed Cross Coupling of Aryl Chlorides with Alkyl Grignard Reagents: Synthetic Scope and FeII/FeIV Mechanism Supported by X-ray Absorption Spectroscopy and Density Functional Theory Calculations Bull. Chem. Soc. Jpn., 92, 2, 381-390 Bull. Chem. Soc. Jpn., 92, 2, 381-390 Bull. Chem. Soc. Jpn., 92, 2, 381-390 2019 Refereed English Disclose to all
Aoki, Y, O’Brien, H. M, Kawasaki, H, Takaya, H, Nakamura, M Aoki, Y, O’Brien, H. M, Kawasaki, H, Takaya, H, Nakamura, M Aoki, Y, O’Brien, H. M, Kawasaki, H, Takaya, H, Nakamura, M Ligand-Free Iron-Catalyzed C–F Amination of Diarylamines: A One-Pot Regioselective Synthesis of Diaryl Dihydrophenazines Ligand-Free Iron-Catalyzed C–F Amination of Diarylamines: A One-Pot Regioselective Synthesis of Diaryl Dihydrophenazines Ligand-Free Iron-Catalyzed C–F Amination of Diarylamines: A One-Pot Regioselective Synthesis of Diaryl Dihydrophenazines Org. Lett., 21, 461-464 Org. Lett., 21, 461-464 Org. Lett., 21, 461-464 2019/01 Refereed English Disclose to all
Isozaki, Katsuhiro, Shimoaka, Takafumi, Oshiro, Satoshi, Yamaguchi, Asako, Pincella, Francesca, Ueno, Ryo, Hasegawa, Takeshi, Watanabe, Takashi, Takaya, Hikaru, Nakamura, Masaharu Isozaki, K, Shimoaka, T, Oshiro, S, Yamaguchi, A, Pincella, F, Ueno, R, Hasegawa, T, Watanabe, T, Takaya, H, Nakamura, M Isozaki, Katsuhiro, Shimoaka, Takafumi, Oshiro, Satoshi, Yamaguchi, Asako, Pincella, Francesca, Ueno, Ryo, Hasegawa, Takeshi, Watanabe, Takashi, Takaya, Hikaru, Nakamura, Masaharu Robust Surface Plasmon Resonance Chips for Repetitive and Accurate Analysis of Lignin-Peptide Interactions Robust Surface Plasmon Resonance Chips for Repetitive and Accurate Analysis of Lignin–Peptide Interactions Robust Surface Plasmon Resonance Chips for Repetitive and Accurate Analysis of Lignin-Peptide Interactions ACS OMEGA, 3, 7, 7483-7493 ACS Omega, 3, 7, 7483-7493 ACS OMEGA, 3, 7, 7483-7493 2018/07 Refereed English Research paper(scientific journal) Disclose to all
Sharma, A. K, Sameera, W. M. C, Adak, L, Jin, M, Okuzono, C, Iwamoto, T, Nakamura, M, Morokuma, K Sharma, A. K, Sameera, W. M. C, Adak, L, Jin, M, Okuzono, C, Iwamoto, T, Nakamura, M, Morokuma, K Sharma, A. K, Sameera, W. M. C, Adak, L, Jin, M, Okuzono, C, Iwamoto, T, Nakamura, M, Morokuma, K DFT and AFIR Study on the Mechanism and the Origin of Enantioselectivity in Iron-Catalyzed Cross-Coupling Reactions DFT and AFIR Study on the Mechanism and the Origin of Enantioselectivity in Iron-Catalyzed Cross-Coupling Reactions DFT and AFIR Study on the Mechanism and the Origin of Enantioselectivity in Iron-Catalyzed Cross-Coupling Reactions J. Am. Chem. Soc., 139, 16117-16125 J. Am. Chem. Soc., 139, 16117-16125 J. Am. Chem. Soc., 139, 16117-16125 2017 Refereed English Disclose to all
Iwamoto, T, Nishikori, T, Nakagawa, N, Takaya, H, Nakamura, M Iwamoto, T, Nishikori, T, Nakagawa, N, Takaya, H, Nakamura, M Iwamoto, T, Nishikori, T, Nakagawa, N, Takaya, H, Nakamura, M Iron-Catalyzed anti-Selective Carbosilylation of Internal Alkynes Iron-Catalyzed anti-Selective Carbosilylation of Internal Alkynes Iron-Catalyzed anti-Selective Carbosilylation of Internal Alkynes Angew. Chem. Int. Ed., 56, 13298-13301 Angew. Chem. Int. Ed., 56, 13298-13301 Angew. Chem. Int. Ed., 56, 13298-13301 2017 Refereed English Disclose to all
Adak, L, Kawamura, S, Toma, G, Takenaka, T, Isozaki, K, Takaya, H, Orita, A, Li, H. C, Shing, T. K. M, Nakamura, M Adak, L, Kawamura, S, Toma, G, Takenaka, T, Isozaki, K, Takaya, H, Orita, A, Li, H. C, Shing, T. K. M, Nakamura, M Adak, L, Kawamura, S, Toma, G, Takenaka, T, Isozaki, K, Takaya, H, Orita, A, Li, H. C, Shing, T. K. M, Nakamura, M Synthesis of Aryl C-Glycosides via Iron-Catalyzed Cross Coupling of Halosugars: Stereoselective Anomeric Arylation of Glycosyl Radicals Synthesis of Aryl C-Glycosides via Iron-Catalyzed Cross Coupling of Halosugars: Stereoselective Anomeric Arylation of Glycosyl Radicals Synthesis of Aryl C-Glycosides via Iron-Catalyzed Cross Coupling of Halosugars: Stereoselective Anomeric Arylation of Glycosyl Radicals J. Am. Chem. Soc., 139, 10693-10701 J. Am. Chem. Soc., 139, 10693-10701 J. Am. Chem. Soc., 139, 10693-10701 2017 Refereed English Disclose to all
Nakajima, S, Takaya, H, Nakamura, M Nakajima, S, Takaya, H, Nakamura, M Nakajima, S, Takaya, H, Nakamura, M Iron-catalyzed Methylation of Arylboron Compounds with Iodomethane Iron-catalyzed Methylation of Arylboron Compounds with Iodomethane Iron-catalyzed Methylation of Arylboron Compounds with Iodomethane Chem. Lett., 46, 5, 711-714 Chem. Lett., 46, 5, 711-714 Chem. Lett., 46, 5, 711-714 2017 Refereed English Disclose to all
Takaya, H, Yokoi, T, Yoshida, R, Isozaki, K, Kawakami, T, Takenaka, T, Nakamura, M Takaya, H, Yokoi, T, Yoshida, R, Isozaki, K, Kawakami, T, Takenaka, T, Nakamura, M Takaya, H, Yokoi, T, Yoshida, R, Isozaki, K, Kawakami, T, Takenaka, T, Nakamura, M Synthesis and Structural Analysis of Ruthenium-bound Norvaline Peptides Synthesis and Structural Analysis of Ruthenium-bound Norvaline Peptides Synthesis and Structural Analysis of Ruthenium-bound Norvaline Peptides Chem. Lett., 46, 5, 665-668 Chem. Lett., 46, 5, 665-668 Chem. Lett., 46, 5, 665-668 2017 Refereed English Disclose to all
Takaya, H, Nakajima, S, Nakamura, M Takaya, H, Nakajima, S, Nakamura, M Takaya, H, Nakajima, S, Nakamura, M Synchrotron X-ray Absorption Spectroscopy and Solution-Phase Structure of Organoiron Catalysts Synchrotron X-ray Absorption Spectroscopy and Solution-Phase Structure of Organoiron Catalysts Synchrotron X-ray Absorption Spectroscopy and Solution-Phase Structure of Organoiron Catalysts CHEMISTRY $ CHEMICAL INDUSTRY,69,391-393 CHEMISTRY $ CHEMICAL INDUSTRY,69,391-393 CHEMISTRY $ CHEMICAL INDUSTRY,69,391-393 2016 Refereed Disclose to all
Isozaki, K, Yokoi, T, Yoshida, R, Ogata, K, Hashizume, D, Yasuda, N, Sadakane, K, Takaya, H, Nakamura, M Isozaki, K, Yokoi, T, Yoshida, R, Ogata, K, Hashizume, D, Yasuda, N, Sadakane, K, Takaya, H, Nakamura, M Isozaki, K, Yokoi, T, Yoshida, R, Ogata, K, Hashizume, D, Yasuda, N, Sadakane, K, Takaya, H, Nakamura, M Synthesis and Applications of ONO-Pincer Ruthenium-Complex-Bound Norvalines Synthesis and Applications of ONO-Pincer Ruthenium-Complex-Bound Norvalines Synthesis and Applications of ONO-Pincer Ruthenium-Complex-Bound Norvalines Chem. Asian. J., 11, 1076-1091 Chem. Asian. J., 11, 1076-1091 Chem. Asian. J., 11, 1076-1091 2016 Refereed English Disclose to all
Yamaguchi, A, Isozaki, K, Nakamura, M, Takaya, H, Watanabe, T Yamaguchi, A, Isozaki, K, Nakamura, M, Takaya, H, Watanabe, T Yamaguchi, A, Isozaki, K, Nakamura, M, Takaya, H, Watanabe, T Discovery of 12-Mer Peptides That Bind to Wood Lignin Discovery of 12-Mer Peptides That Bind to Wood Lignin Discovery of 12-Mer Peptides That Bind to Wood Lignin Scientific Reports, 6, 21833 Scientific Reports, 6, 21833 Scientific Reports, 6, 21833 2016 Refereed English Disclose to all
Yoshida, R, Isozaki, K, Yokoi, T, Yasuda, N, Sadakane, K, Iwamoto, T, Takaya, H, Nakamura. M Yoshida, R, Isozaki, K, Yokoi, T, Yasuda, N, Sadakane, K, Iwamoto, T, Takaya, H, Nakamura. M Yoshida, R, Isozaki, K, Yokoi, T, Yasuda, N, Sadakane, K, Iwamoto, T, Takaya, H, Nakamura. M ONO-Pincer Ruthenium Complex-Bound Norvaline for Efficient Catalytic Oxidation of Methoxybenzenes with Hydrogen Peroxide ONO-Pincer Ruthenium Complex-Bound Norvaline for Efficient Catalytic Oxidation of Methoxybenzenes with Hydrogen Peroxide ONO-Pincer Ruthenium Complex-Bound Norvaline for Efficient Catalytic Oxidation of Methoxybenzenes with Hydrogen Peroxide Org. Biomol. Chem., 14, 31, 7468-7479 Org. Biomol. Chem., 14, 31, 7468-7479 Org. Biomol. Chem., 14, 31, 7468-7479 2016 Refereed English Disclose to all
S. Kawamura, R. Agata, M. Nakamura S. Kawamura, R. Agata, M. Nakamura S. Kawamura, R. Agata, M. Nakamura Regio- and stereoselective multisubstituted olefin synthesis via hydro/carboalumination of alkynes and subsequent iron-catalysed cross-coupling reaction with alkyl halides Regio- and stereoselective multisubstituted olefin synthesis via hydro/carboalumination of alkynes and subsequent iron-catalysed cross-coupling reaction with alkyl halides Regio- and stereoselective multisubstituted olefin synthesis via hydro/carboalumination of alkynes and subsequent iron-catalysed cross-coupling reaction with alkyl halides Organic Chemistry Frontiers, 2, 9, 1053-1058 Organic Chemistry Frontiers, 2, 9, 1053-1058 Organic Chemistry Frontiers, 2, 9, 1053-1058 2015/06 Refereed English Disclose to all
M. Jin, L. Adak, M. Nakamura M. Jin, L. Adak, M. Nakamura M. Jin, L. Adak, M. Nakamura Iron-Catalyzed Enantioselective Cross-Coupling Reactions of α-Chloroesters with Aryl Grignard Reagents Iron-Catalyzed Enantioselective Cross-Coupling Reactions of α-Chloroesters with Aryl Grignard Reagents Iron-Catalyzed Enantioselective Cross-Coupling Reactions of α-Chloroesters with Aryl Grignard Reagents Journal of the American Chemical Society, 137, 22, 7128-7134 Journal of the American Chemical Society, 137, 22, 7128-7134 Journal of the American Chemical Society, 137, 22, 7128-7134 2015/05 Refereed English Disclose to all
Aoki, Y., Imayoshi, R., Hatakeyama, T., Takaya, H., Nakamuraa, M. Aoki, Y., Imayoshi, R., Hatakeyama, T., Takaya, H., Nakamuraa, M. Aoki, Y., Imayoshi, R., Hatakeyama, T., Takaya, H., Nakamuraa, M. Synthesis of 2,7-disubstituted 5,10-diaryl-5,10-dihydrophenazines via iron-catalyzed intramolecular ring-closing C-H amination Synthesis of 2,7-disubstituted 5,10-diaryl-5,10-dihydrophenazines via iron-catalyzed intramolecular ring-closing C-H amination Synthesis of 2,7-disubstituted 5,10-diaryl-5,10-dihydrophenazines via iron-catalyzed intramolecular ring-closing C-H amination Heterocycles, 90, 2, 893-900 Heterocycles, 90, 2, 893-900 Heterocycles, 90, 2, 893-900 2015 Refereed English Research paper(scientific journal) Disclose to all
Takaya, H., Nakajima, S., Nakagawa, N., Isozaki, K., Iwamoto, T., Imayoshi, R., Gower, N.J., Adak, L., Hatakeyama, T., Honma, T., Takagaki, M., Sunada, Y., Nagashima, H., Hashizume, D., Takahashi, O., Nakamura, M. Takaya, H., Nakajima, S., Nakagawa, N., Isozaki, K., Iwamoto, T., Imayoshi, R., Gower, N.J., Adak, L., Hatakeyama, T., Honma, T., Takagaki, M., Sunada, Y., Nagashima, H., Hashizume, D., Takahashi, O., Nakamura, M. Takaya, H., Nakajima, S., Nakagawa, N., Isozaki, K., Iwamoto, T., Imayoshi, R., Gower, N.J., Adak, L., Hatakeyama, T., Honma, T., Takagaki, M., Sunada, Y., Nagashima, H., Hashizume, D., Takahashi, O., Nakamura, M. Investigation of organoiron catalysis in Kumada-Tamao-Corriu-type cross-coupling reaction assisted by solution-phase X-ray absorption spectroscopy Investigation of organoiron catalysis in Kumada-Tamao-Corriu-type cross-coupling reaction assisted by solution-phase X-ray absorption spectroscopy Investigation of organoiron catalysis in Kumada-Tamao-Corriu-type cross-coupling reaction assisted by solution-phase X-ray absorption spectroscopy Bulletin of the Chemical Society of Japan, 88, 3, 410-418 Bulletin of the Chemical Society of Japan, 88, 3, 410-418 Bulletin of the Chemical Society of Japan, 88, 3, 410-418 2015 Refereed English Research paper(scientific journal) Disclose to all
Nakagawa, N., Hatakeyama, T., Nakamura, M. Nakagawa, N., Hatakeyama, T., Nakamura, M. Nakagawa, N., Hatakeyama, T., Nakamura, M. Iron-catalyzed diboration and carboboration of alkynes Iron-catalyzed diboration and carboboration of alkynes Iron-catalyzed diboration and carboboration of alkynes Chemistry - A European Journal, 21, 11, 4257-4261 Chemistry - A European Journal, 21, 11, 4257-4261 Chemistry - A European Journal, 21, 11, 4257-4261 2015 Refereed English Research paper(scientific journal) Disclose to all
Nakagawa, N., Hatakeyama, T., Nakamura, M. Nakagawa, N., Hatakeyama, T., Nakamura, M. Nakagawa, N., Hatakeyama, T., Nakamura, M. Iron-catalyzed Suzuki-Miyaura coupling reaction of unactivated alkyl halides with lithium alkynylborates Iron-catalyzed Suzuki-Miyaura coupling reaction of unactivated alkyl halides with lithium alkynylborates Iron-catalyzed Suzuki-Miyaura coupling reaction of unactivated alkyl halides with lithium alkynylborates Chemistry Letters, 44, 4, 486-488 Chemistry Letters, 44, 4, 486-488 Chemistry Letters, 44, 4, 486-488 2015 Refereed English Research paper(scientific journal) Disclose to all
Agata, R., Iwamoto, T., Nakagawa, N., Isozaki, K., Hatakeyama, T., Takaya, H., Nakamura, M. R. Agata, T. Iwamoto, N. Nakagawa, K. Isozak, T. Hatakeyama, H. Takaya, M. Nakamura Agata, R., Iwamoto, T., Nakagawa, N., Isozaki, K., Hatakeyama, T., Takaya, H., Nakamura, M. Iron fluoride/N-heterocyclic carbene catalyzed cross coupling between deactivated aryl chlorides and alkyl grignard reagents with or without β-hydrogens Iron Fluoride/N-Heterocyclic Carbene Catalyzed Cross Coupling_ between Deactivated Aryl Chlorides and Alkyl Grignard Reagents with or without β-Hydrogens Iron fluoride/N-heterocyclic carbene catalyzed cross coupling between deactivated aryl chlorides and alkyl grignard reagents with or without β-hydrogens Synthesis (Germany), 47, 12, 1733-1740 Synthesis, 47, 12, 1733-1740 Synthesis (Germany), 47, 12, 1733-1740 2015 Refereed English Research paper(scientific journal) Disclose to all
Hashimoto, S., Nakatsuka, S., Nakamura, M., Hatakeyama, T. Hashimoto, S., Nakatsuka, S., Nakamura, M., Hatakeyama, T. Hashimoto, S., Nakatsuka, S., Nakamura, M., Hatakeyama, T. Construction of a highly distorted benzene ring in a double helicene Construction of a highly distorted benzene ring in a double helicene Construction of a highly distorted benzene ring in a double helicene Angewandte Chemie - International Edition, 53, 51, 14074-14076 Angewandte Chemie - International Edition, 53, 51, 14074-14076 Angewandte Chemie - International Edition, 53, 51, 14074-14076 2014 Refereed English Research paper(scientific journal) Disclose to all
Hashimoto, S., Ikuta, T., Shiren, K., Nakatsuka, S., Ni, J., Nakamura, M., Hatakeyama, T. Hashimoto, S., Ikuta, T., Shiren, K., Nakatsuka, S., Ni, J., Nakamura, M., Hatakeyama, T. Hashimoto, S., Ikuta, T., Shiren, K., Nakatsuka, S., Ni, J., Nakamura, M., Hatakeyama, T. Triplet-energy control of polycyclic aromatic hydrocarbons by BN replacement: Development of ambipolar host materials for phosphorescent organic light-emitting diodes Triplet-energy control of polycyclic aromatic hydrocarbons by BN replacement: Development of ambipolar host materials for phosphorescent organic light-emitting diodes Triplet-energy control of polycyclic aromatic hydrocarbons by BN replacement: Development of ambipolar host materials for phosphorescent organic light-emitting diodes Chemistry of Materials, 26, 21, 6265-6271 Chemistry of Materials, 26, 21, 6265-6271 Chemistry of Materials, 26, 21, 6265-6271 2014 Refereed English Research paper(scientific journal) Disclose to all
S. Azuma, M. Ota, A. Ishida, K. Isozaki, H. Takaya, M. Nakamura, T. Sasamori, N. Tokitoh, K. Kuramochi, K. Tsubaki S. Azuma, M. Ota, A. Ishida, K. Isozaki, H. Takaya, M. Nakamura, T. Sasamori, N. Tokitoh, K. Kuramochi, K. Tsubaki S. Azuma, M. Ota, A. Ishida, K. Isozaki, H. Takaya, M. Nakamura, T. Sasamori, N. Tokitoh, K. Kuramochi, K. Tsubaki Dimerization Reactions of 2-Bromo-3,5,6-Trimethyl-1,4-Benzoquinone Dimerization Reactions of 2-Bromo-3,5,6-Trimethyl-1,4-Benzoquinone Dimerization Reactions of 2-Bromo-3,5,6-Trimethyl-1,4-Benzoquinone Chemistry Letters, 42, 12, 1531-1533 Chemistry Letters, 42, 12, 1531-1533 Chemistry Letters, 42, 12, 1531-1533 2013/09 Refereed English Disclose to all
S. Kawamura, M. Nakamura S. Kawamura, M. Nakamura S. Kawamura, M. Nakamura Ligand-controlled iron-catalyzed cross coupling of benzylic chlorides with aryl Grignard reagents Ligand-controlled iron-catalyzed cross coupling of benzylic chlorides with aryl Grignard reagents Ligand-controlled iron-catalyzed cross coupling of benzylic chlorides with aryl Grignard reagents Chemistry Letters, 42, 2, 183-185 Chemistry Letters, 42, 2, 183-185 Chemistry Letters, 42, 2, 183-185 2013/02 Refereed English Disclose to all
M. Jin, M. Nakamura M. Jin, M. Nakamura M. Jin, M. Nakamura Synthesis of novel C2 and C1 symmetric chiraphos derivatives and their application in palladium-catalyzed miyauramichael reaction Synthesis of novel C2 and C1 symmetric chiraphos derivatives and their application in palladium-catalyzed miyauramichael reaction Synthesis of novel C2 and C1 symmetric chiraphos derivatives and their application in palladium-catalyzed miyauramichael reaction Chemistry Letters, 42, 9, 1035-1037 Chemistry Letters, 42, 9, 1035-1037 Chemistry Letters, 42, 9, 1035-1037 2013 Refereed English Disclose to all
Gabr, R.K., Hatakeyama, T., Takenaka, K., Takizawa, S., Okada, Y., Nakamura, M., Sasai, H. Gabr, R.K., Hatakeyama, T., Takenaka, K., Takizawa, S., Okada, Y., Nakamura, M., Sasai, H. Gabr, R.K., Hatakeyama, T., Takenaka, K., Takizawa, S., Okada, Y., Nakamura, M., Sasai, H. DFT study of a 5-endo-trig-type cyclization of 3-alkenoic acids by using Pd-spiro-bis(isoxazoline) as catalyst: Importance of the rigid spiro framework for both selectivity and reactivity DFT study of a 5-endo-trig-type cyclization of 3-alkenoic acids by using Pd-spiro-bis(isoxazoline) as catalyst: Importance of the rigid spiro framework for both selectivity and reactivity DFT study of a 5-endo-trig-type cyclization of 3-alkenoic acids by using Pd-spiro-bis(isoxazoline) as catalyst: Importance of the rigid spiro framework for both selectivity and reactivity Chemistry - A European Journal, 19, 29, 9518-9525 Chemistry - A European Journal, 19, 29, 9518-9525 Chemistry - A European Journal, 19, 29, 9518-9525 2013 Refereed English Research paper(scientific journal) Disclose to all
H. Takaya, T. Iwaya, K. Ogata, K. Isozaki, T. Yokoi, R. Yoshida, N. Yasuda, H. Seike, T. Takenaka, M. Nakamura H. Takaya, T. Iwaya, K. Ogata, K. Isozaki, T. Yokoi, R. Yoshida, N. Yasuda, H. Seike, T. Takenaka, M. Nakamura H. Takaya, T. Iwaya, K. Ogata, K. Isozaki, T. Yokoi, R. Yoshida, N. Yasuda, H. Seike, T. Takenaka, M. Nakamura Synthesis, structure, and function of pcp pincer transition-metal-complex- bound norvaline derivatives Synthesis, structure, and function of pcp pincer transition-metal-complex- bound norvaline derivatives Synthesis, structure, and function of pcp pincer transition-metal-complex- bound norvaline derivatives Synlett, 24, 15, 1910-1914 Synlett, 24, 15, 1910-1914 Synlett, 24, 15, 1910-1914 2013 Refereed English Disclose to all
K. Ogata, D. Sasano, T. Yokoi, K. Isozaki, R. Yoshida, T. Takenaka, H. Seike, T. Ogawa, H. Kurata, N. Yasuda, H. Takaya, M. Nakamura K. Ogata, D. Sasano, T. Yokoi, K. Isozaki, R. Yoshida, T. Takenaka, H. Seike, T. Ogawa, H. Kurata, N. Yasuda, H. Takaya, M. Nakamura K. Ogata, D. Sasano, T. Yokoi, K. Isozaki, R. Yoshida, T. Takenaka, H. Seike, T. Ogawa, H. Kurata, N. Yasuda, H. Takaya, M. Nakamura Synthesis and self-assembly of NCN-pincer Pd-complex-bound norvalines Synthesis and self-assembly of NCN-pincer Pd-complex-bound norvalines Synthesis and self-assembly of NCN-pincer Pd-complex-bound norvalines Chemistry - A European Journal, 19, 37, 12356-12375 Chemistry - A European Journal, 19, 37, 12356-12375 Chemistry - A European Journal, 19, 37, 12356-12375 2013 Refereed English Disclose to all
Kazuhiro Fukami, Ryo Koda, Tetsuo Sakka, Tomoko Urata, Ken Ichi Amano, Hikaru Takaya, Masaharu Nakamura, Yukio Ogata, Masahiro Kinoshita Kazuhiro Fukami, Ryo Koda, Tetsuo Sakka, Tomoko Urata, Ken Ichi Amano, Hikaru Takaya, Masaharu Nakamura, Yukio Ogata, Masahiro Kinoshita Kazuhiro Fukami, Ryo Koda, Tetsuo Sakka, Tomoko Urata, Ken Ichi Amano, Hikaru Takaya, Masaharu Nakamura, Yukio Ogata, Masahiro Kinoshita Platinum electrodeposition in porous silicon: The influence of surface solvation effects on a chemical reaction in a nanospace Platinum electrodeposition in porous silicon: The influence of surface solvation effects on a chemical reaction in a nanospace Platinum electrodeposition in porous silicon: The influence of surface solvation effects on a chemical reaction in a nanospace Chemical Physics Letters, 542, 99-105 Chemical Physics Letters, 542, 99-105 Chemical Physics Letters, 542, 99-105 2012/07/23 Refereed English Research paper(scientific journal) Disclose to all
K. Ogata, D. Sasano, T. Yokoi, K. Isozaki, H. Seike, H. Takaya, M. Nakamura K. Ogata, D. Sasano, T. Yokoi, K. Isozaki, H. Seike, H. Takaya, M. Nakamura K. Ogata, D. Sasano, T. Yokoi, K. Isozaki, H. Seike, H. Takaya, M. Nakamura Pd-complex-bound amino acid-based supramolecular gel catalyst for intramolecular additioncyclization of alkynoic acids in water Pd-complex-bound amino acid-based supramolecular gel catalyst for intramolecular additioncyclization of alkynoic acids in water Pd-complex-bound amino acid-based supramolecular gel catalyst for intramolecular additioncyclization of alkynoic acids in water Chemistry Letters, 41, 5, 498-500 Chemistry Letters, 41, 5, 498-500 Chemistry Letters, 41, 5, 498-500 2012/05 Refereed English Disclose to all
Ogata, Kazuki, Sasano, Daisuke, Yokoi, Tomoya, Isozaki, Katsuhiro, Seike, Hirofumi, Yasuda, Nobuhiro, Ogawa, Tetsuya, Kurata, Hiroki, Takaya, Hikaru, Nakamura, Masaharu Ogata, Kazuki, Sasano, Daisuke, Yokoi, Tomoya, Isozaki, Katsuhiro, Seike, Hirofumi, Yasuda, Nobuhiro, Ogawa, Tetsuya, Kurata, Hiroki, Takaya, Hikaru, Nakamura, Masaharu Ogata, Kazuki, Sasano, Daisuke, Yokoi, Tomoya, Isozaki, Katsuhiro, Seike, Hirofumi, Yasuda, Nobuhiro, Ogawa, Tetsuya, Kurata, Hiroki, Takaya, Hikaru, Nakamura, Masaharu Synthesis and Supramolecular Association of NCN-Pincer Pd-Complex-bound Norvaline Derivatives toward Fabrication of Controlled Metal Array Synthesis and Supramolecular Association of NCN-Pincer Pd-Complex-bound Norvaline Derivatives toward Fabrication of Controlled Metal Array Synthesis and Supramolecular Association of NCN-Pincer Pd-Complex-bound Norvaline Derivatives toward Fabrication of Controlled Metal Array CHEMISTRY LETTERS, 41, 2, 194-196 CHEMISTRY LETTERS, 41, 2, 194-196 CHEMISTRY LETTERS, 41, 2, 194-196 2012/02 Refereed English Disclose to all
Hatakeyama, T., Imayoshi, R., Yoshimoto, Y., Ghorai, S.K., Jin, M., Takaya, H., Norisuye, K., Sohrin, Y., Nakamura, M. Hatakeyama, T., Imayoshi, R., Yoshimoto, Y., Ghorai, S.K., Jin, M., Takaya, H., Norisuye, K., Sohrin, Y., Nakamura, M. Hatakeyama, T., Imayoshi, R., Yoshimoto, Y., Ghorai, S.K., Jin, M., Takaya, H., Norisuye, K., Sohrin, Y., Nakamura, M. Iron-catalyzed aromatic amination for nonsymmetrical triarylamine synthesis Iron-catalyzed aromatic amination for nonsymmetrical triarylamine synthesis Iron-catalyzed aromatic amination for nonsymmetrical triarylamine synthesis Journal of the American Chemical Society, 134, 50, 20262-20265 Journal of the American Chemical Society, 134, 50, 20262-20265 Journal of the American Chemical Society, 134, 50, 20262-20265 2012 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Hashimoto, S., Oba, T., Nakamura, M. Hatakeyama, T., Hashimoto, S., Oba, T., Nakamura, M. Hatakeyama, T., Hashimoto, S., Oba, T., Nakamura, M. Azaboradibenzo[6]helicene: Carrier inversion induced by helical homochirality Azaboradibenzo[6]helicene: Carrier inversion induced by helical homochirality Azaboradibenzo[6]helicene: Carrier inversion induced by helical homochirality Journal of the American Chemical Society, 134, 48, 19600-19603 Journal of the American Chemical Society, 134, 48, 19600-19603 Journal of the American Chemical Society, 134, 48, 19600-19603 2012 Refereed English Research paper(scientific journal) Disclose to all
K. Isozaki, K. Ogata, Y. Haga, D. Sasano, T. Ogawa, H. Kurata, M. Nakamura, T. Naota, H. Takaya K. Isozaki, K. Ogata, Y. Haga, D. Sasano, T. Ogawa, H. Kurata, M. Nakamura, T. Naota, H. Takaya K. Isozaki, K. Ogata, Y. Haga, D. Sasano, T. Ogawa, H. Kurata, M. Nakamura, T. Naota, H. Takaya Metal array fabrication through self-assembly of Pt-complex-bound amino acids Metal array fabrication through self-assembly of Pt-complex-bound amino acids Metal array fabrication through self-assembly of Pt-complex-bound amino acids Chemical Communications, 48, 33, 3936-3938 Chemical Communications, 48, 33, 3936-3938 Chemical Communications, 48, 33, 3936-3938 2012 Refereed English Disclose to all
Noda, D., Sunada, Y., Hatakeyama, T., Nakamura, M., Nagashima, H. Noda, D., Sunada, Y., Hatakeyama, T., Nakamura, M., Nagashima, H. Noda, D., Sunada, Y., Hatakeyama, T., Nakamura, M., Nagashima, H. Iron promoted conjugate addition: Implication of the six-centered mechanism based on the isolation of the iron-enolate intermediate Iron promoted conjugate addition: Implication of the six-centered mechanism based on the isolation of the iron-enolate intermediate Iron promoted conjugate addition: Implication of the six-centered mechanism based on the isolation of the iron-enolate intermediate Chemical Communications, 48, 100, 12231-12233 Chemical Communications, 48, 100, 12231-12233 Chemical Communications, 48, 100, 12231-12233 2012 Refereed English Research paper(scientific journal) Disclose to all
H. Nishimura, M. Sasaki, H. Seike, M. Nakamura, T. Watanabe H. Nishimura, M. Sasaki, H. Seike, M. Nakamura, T. Watanabe H. Nishimura, M. Sasaki, H. Seike, M. Nakamura, T. Watanabe Alkadienyl and alkenyl itaconic acids (ceriporic acids G and H) from the selective white-rot fungus Ceriporiopsis subvermispora: A new class of metabolites initiating ligninolytic lipid peroxidation Alkadienyl and alkenyl itaconic acids (ceriporic acids G and H) from the selective white-rot fungus Ceriporiopsis subvermispora: A new class of metabolites initiating ligninolytic lipid peroxidation Alkadienyl and alkenyl itaconic acids (ceriporic acids G and H) from the selective white-rot fungus Ceriporiopsis subvermispora: A new class of metabolites initiating ligninolytic lipid peroxidation Organic and Biomolecular Chemistry, 10, 31, 6432-6442 Organic and Biomolecular Chemistry, 10, 31, 6432-6442 Organic and Biomolecular Chemistry, 10, 31, 6432-6442 2012 Refereed English Disclose to all
S. Kawamura, T. Kawabata, K. Ishizuka, M. Nakamura S. Kawamura, T. Kawabata, K. Ishizuka, M. Nakamura S. Kawamura, T. Kawabata, K. Ishizuka, M. Nakamura Iron-catalysed cross-coupling of halohydrins with aryl aluminium reagents: A protecting-group-free strategy attaining remarkable rate enhancement and diastereoinduction Iron-catalysed cross-coupling of halohydrins with aryl aluminium reagents: A protecting-group-free strategy attaining remarkable rate enhancement and diastereoinduction Iron-catalysed cross-coupling of halohydrins with aryl aluminium reagents: A protecting-group-free strategy attaining remarkable rate enhancement and diastereoinduction Chemical Communications, 48, 75, 9376-9378 Chemical Communications, 48, 75, 9376-9378 Chemical Communications, 48, 75, 9376-9378 2012 Refereed English Disclose to all
Hatakeyama, T., Hashimoto, T., Kathriarachchi, K.K.A.D.S., Zenmyo, T., Seike, H., Nakamura, M. Hatakeyama, T., Hashimoto, T., Kathriarachchi, K.K.A.D.S., Zenmyo, T., Seike, H., Nakamura, M. Hatakeyama, T., Hashimoto, T., Kathriarachchi, K.K.A.D.S., Zenmyo, T., Seike, H., Nakamura, M. Iron-catalyzed alkyl-alkyl Suzuki-Miyaura coupling Iron-catalyzed alkyl-alkyl Suzuki-Miyaura coupling Iron-catalyzed alkyl-alkyl Suzuki-Miyaura coupling Angewandte Chemie - International Edition, 51, 35, 8834-8837 Angewandte Chemie - International Edition, 51, 35, 8834-8837 Angewandte Chemie - International Edition, 51, 35, 8834-8837 2012 Refereed English Research paper(scientific journal) Disclose to all
Hashimoto, T., Hatakeyama, T., Nakamura, M. Hashimoto, T., Hatakeyama, T., Nakamura, M. Hashimoto, T., Hatakeyama, T., Nakamura, M. Stereospecific cross-coupling between alkenylboronates and alkyl halides catalyzed by iron-bisphosphine complexes Stereospecific cross-coupling between alkenylboronates and alkyl halides catalyzed by iron-bisphosphine complexes Stereospecific cross-coupling between alkenylboronates and alkyl halides catalyzed by iron-bisphosphine complexes Journal of Organic Chemistry, 77, 2, 1168-1173 Journal of Organic Chemistry, 77, 2, 1168-1173 Journal of Organic Chemistry, 77, 2, 1168-1173 2012 Refereed English Research paper(scientific journal) Disclose to all
Ghorai, S.K., Jin, M., Hatakeyama, T., Nakamura, M. Ghorai, S.K., Jin, M., Hatakeyama, T., Nakamura, M. Ghorai, S.K., Jin, M., Hatakeyama, T., Nakamura, M. Cross-coupling of non-activated chloroalkanes with aryl grignard reagents in the presence of iron/N-heterocyclic carbene catalysts Cross-coupling of non-activated chloroalkanes with aryl grignard reagents in the presence of iron/N-heterocyclic carbene catalysts Cross-coupling of non-activated chloroalkanes with aryl grignard reagents in the presence of iron/N-heterocyclic carbene catalysts Organic Letters, 14, 4, 1066-1069 Organic Letters, 14, 4, 1066-1069 Organic Letters, 14, 4, 1066-1069 2012 Refereed English Research paper(scientific journal) Disclose to all
M. Jin, M. Nakamura M. Jin, M. Nakamura M. Jin, M. Nakamura Iron-catalyzed chemoselective cross-coupling of α-bromocarboxylic acid derivatives with aryl grignard reagents Iron-catalyzed chemoselective cross-coupling of α-bromocarboxylic acid derivatives with aryl grignard reagents Iron-catalyzed chemoselective cross-coupling of α-bromocarboxylic acid derivatives with aryl grignard reagents Chemistry Letters, 40, 9, 1012-1014 Chemistry Letters, 40, 9, 1012-1014 Chemistry Letters, 40, 9, 1012-1014 2011/09 Refereed English Disclose to all
Hatakeyama, T., Fujiwara, Y.-I., Okada, Y., Itoh, T., Hashimoto, T., Kawamura, S., Ogata, K., Takaya, H., Nakamura, M. Hatakeyama, T., Fujiwara, Y.-I., Okada, Y., Itoh, T., Hashimoto, T., Kawamura, S., Ogata, K., Takaya, H., Nakamura, M. Hatakeyama, T., Fujiwara, Y.-I., Okada, Y., Itoh, T., Hashimoto, T., Kawamura, S., Ogata, K., Takaya, H., Nakamura, M. Kumadatamaocorriu coupling of alkyl halides catalyzed by an ironbisphosphine complex Kumadatamaocorriu coupling of alkyl halides catalyzed by an ironbisphosphine complex Kumadatamaocorriu coupling of alkyl halides catalyzed by an ironbisphosphine complex Chemistry Letters, 40, 9, 1030-1032 Chemistry Letters, 40, 9, 1030-1032 Chemistry Letters, 40, 9, 1030-1032 2011 Refereed English Research paper(scientific journal) Disclose to all
S. Ito, T. Itoh, M. Nakamura S. Ito, T. Itoh, M. Nakamura S. Ito, T. Itoh, M. Nakamura Diastereoselective carbometalation of Oxa- and azabicyclic alkenes under iron catalysis Diastereoselective carbometalation of Oxa- and azabicyclic alkenes under iron catalysis Diastereoselective carbometalation of Oxa- and azabicyclic alkenes under iron catalysis Angewandte Chemie - International Edition, 50, 2, 454-457 Angewandte Chemie - International Edition, 50, 2, 454-457 Angewandte Chemie - International Edition, 50, 2, 454-457 2011 Refereed English Disclose to all
Hatakeyama, T., Okada, Y., Yoshimoto, Y., Nakamura, M. Hatakeyama, T., Okada, Y., Yoshimoto, Y., Nakamura, M. Hatakeyama, T., Okada, Y., Yoshimoto, Y., Nakamura, M. Tuning chemoselectivity in iron-catalyzed sonogashira-type reactions using a bisphosphine ligand with peripheral steric bulk: Selective alkynylation of nonactivated alkyl halides Tuning chemoselectivity in iron-catalyzed sonogashira-type reactions using a bisphosphine ligand with peripheral steric bulk: Selective alkynylation of nonactivated alkyl halides Tuning chemoselectivity in iron-catalyzed sonogashira-type reactions using a bisphosphine ligand with peripheral steric bulk: Selective alkynylation of nonactivated alkyl halides Angewandte Chemie - International Edition, 50, 46, 10973-10976 Angewandte Chemie - International Edition, 50, 46, 10973-10976 Angewandte Chemie - International Edition, 50, 46, 10973-10976 2011 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Hashimoto, S., Nakamura, M. T. Hatakeyama, S. Hashimoto, M. Nakamura Hatakeyama, T., Hashimoto, S., Nakamura, M. Tandem phospha-friedel-crafts reaction toward curved π-conjugated frameworks with a phosphorus ring junction Tandem phospha-friedel-crafts reaction toward curved π-conjugated frameworks with a phosphorus ring junction Tandem phospha-friedel-crafts reaction toward curved π-conjugated frameworks with a phosphorus ring junction Organic Letters, 13, 8, 2130-2133 Organic Letters, 13, 8, 2130-2133 Organic Letters, 13, 8, 2130-2133 2011 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Hashimoto, S., Seki, S., Nakamura, M. Hatakeyama, T., Hashimoto, S., Seki, S., Nakamura, M. Hatakeyama, T., Hashimoto, S., Seki, S., Nakamura, M. Synthesis of BN-fused polycyclic aromatics via tandem intramolecular electrophilic arene borylation Synthesis of BN-fused polycyclic aromatics via tandem intramolecular electrophilic arene borylation Synthesis of BN-fused polycyclic aromatics via tandem intramolecular electrophilic arene borylation Journal of the American Chemical Society, 133, 46, 18614-18617 Journal of the American Chemical Society, 133, 46, 18614-18617 Journal of the American Chemical Society, 133, 46, 18614-18617 2011 Refereed English Research paper(scientific journal) Disclose to all
Ishizuka, K., Seike, H., Hatakeyama, T., Nakamura, M. Ishizuka, K., Seike, H., Hatakeyama, T., Nakamura, M. Ishizuka, K., Seike, H., Hatakeyama, T., Nakamura, M. Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides Nickel-catalyzed alkenylative cross-coupling reaction of alkyl sulfides Journal of the American Chemical Society, 132, 38, 13117-13119 Journal of the American Chemical Society, 132, 38, 13117-13119 Journal of the American Chemical Society, 132, 38, 13117-13119 2010 Refereed English Research paper(scientific journal) Disclose to all
S. Kawamura, K. Ishizuka, H. Takaya, M. Nakamura S. Kawamura, K. Ishizuka, H. Takaya, M. Nakamura S. Kawamura, K. Ishizuka, H. Takaya, M. Nakamura The first iron-catalysed aluminium-variant Negishi coupling: Critical effect of co-existing salts on the dynamic equilibrium of arylaluminium species and their reactivity The first iron-catalysed aluminium-variant Negishi coupling: Critical effect of co-existing salts on the dynamic equilibrium of arylaluminium species and their reactivity The first iron-catalysed aluminium-variant Negishi coupling: Critical effect of co-existing salts on the dynamic equilibrium of arylaluminium species and their reactivity Chemical Communications, 46, 33, 6054-6056 Chemical Communications, 46, 33, 6054-6056 Chemical Communications, 46, 33, 6054-6056 2010 Refereed English Disclose to all
Hatakeyama, T., Yoshimoto, Y., Ghorai, S.K., Nakamura, M. Hatakeyama, T., Yoshimoto, Y., Ghorai, S.K., Nakamura, M. Hatakeyama, T., Yoshimoto, Y., Ghorai, S.K., Nakamura, M. Transition-metal-free electrophilic amination between aryl grignard reagents and N-chloroamines Transition-metal-free electrophilic amination between aryl grignard reagents and N-chloroamines Transition-metal-free electrophilic amination between aryl grignard reagents and N-chloroamines Organic Letters, 12, 7, 1516-1519 Organic Letters, 12, 7, 1516-1519 Organic Letters, 12, 7, 1516-1519 2010 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Hashimoto, T., Kondo, Y., Fujiwara, Y., Seike, H., Takaya, H., Tamada, Y., Ono, T., Nakamura, M. Hatakeyama, T., Hashimoto, T., Kondo, Y., Fujiwara, Y., Seike, H., Takaya, H., Tamada, Y., Ono, T., Nakamura, M. Hatakeyama, T., Hashimoto, T., Kondo, Y., Fujiwara, Y., Seike, H., Takaya, H., Tamada, Y., Ono, T., Nakamura, M. Iron-catalyzed Suzuki-Miyaura coupling of alkyl halides Iron-catalyzed Suzuki-Miyaura coupling of alkyl halides Iron-catalyzed Suzuki-Miyaura coupling of alkyl halides Journal of the American Chemical Society, 132, 31, 10674-10676 Journal of the American Chemical Society, 132, 31, 10674-10676 Journal of the American Chemical Society, 132, 31, 10674-10676 2010 Refereed English Research paper(scientific journal) Disclose to all
R.B. Bedford, M. Nakamura, N.J. Gower, M.F. Haddow, M.A. Hall, M. Huwe, T. Hashimoto, R.A. Okopie R.B. Bedford, M. Nakamura, N.J. Gower, M.F. Haddow, M.A. Hall, M. Huwe, T. Hashimoto, R.A. Okopie R.B. Bedford, M. Nakamura, N.J. Gower, M.F. Haddow, M.A. Hall, M. Huwe, T. Hashimoto, R.A. Okopie Iron-catalysed Suzuki coupling? A cautionary tale Iron-catalysed Suzuki coupling? A cautionary tale Iron-catalysed Suzuki coupling? A cautionary tale Tetrahedron Letters, 50, 45, 6110-6111 Tetrahedron Letters, 50, 45, 6110-6111 Tetrahedron Letters, 50, 45, 6110-6111 2009/11 Refereed English Disclose to all
S. Ito, Y.-I. Fujiwara, E. Nakamura, M. Nakamura S. Ito, Y.-I. Fujiwara, E. Nakamura, M. Nakamura S. Ito, Y.-I. Fujiwara, E. Nakamura, M. Nakamura Iron-catalyzed cross-coupling of alkyl sulfonates with arylzinc reagents Iron-catalyzed cross-coupling of alkyl sulfonates with arylzinc reagents Iron-catalyzed cross-coupling of alkyl sulfonates with arylzinc reagents Organic Letters, 11, 19, 4306-4309 Organic Letters, 11, 19, 4306-4309 Organic Letters, 11, 19, 4306-4309 2009/10 Refereed English Disclose to all
Hatakeyama, T., Nakagawa, N., Nakamura, M. Hatakeyama, T., Nakagawa, N., Nakamura, M. Hatakeyama, T., Nakagawa, N., Nakamura, M. Iron-catalyzed negishi coupling toward an effective olefin synthesis Iron-catalyzed negishi coupling toward an effective olefin synthesis Iron-catalyzed negishi coupling toward an effective olefin synthesis Organic Letters, 11, 20, 4496-4499 Organic Letters, 11, 20, 4496-4499 Organic Letters, 11, 20, 4496-4499 2009 Refereed English Research paper(scientific journal) Disclose to all
T. Fujimoto, K. Endo, M. Nakamura, E. Nakamura, M. Webster, J.A. Ragan T. Fujimoto, K. Endo, M. Nakamura, E. Nakamura, M. Webster, J.A. Ragan T. Fujimoto, K. Endo, M. Nakamura, E. Nakamura, M. Webster, J.A. Ragan Synthesis of ethyl 2-ethanoyl-2-methyl-3-phenylbut-3-enoate Synthesis of ethyl 2-ethanoyl-2-methyl-3-phenylbut-3-enoate Synthesis of ethyl 2-ethanoyl-2-methyl-3-phenylbut-3-enoate Organic Syntheses, 86, 325-332 Organic Syntheses, 86, 325-332 Organic Syntheses, 86, 325-332 2009 Refereed English Disclose to all
K. Ishizuka, D. Ando, T. Watanabe, M. Nakamura K. Ishizuka, D. Ando, T. Watanabe, M. Nakamura K. Ishizuka, D. Ando, T. Watanabe, M. Nakamura threo-2-(2,6-Dimethoxy-phen-oxy)-1-(4-eth-oxy-3-methoxy-phen-yl)propane-1, 3-diol threo-2-(2,6-Dimethoxy-phen-oxy)-1-(4-eth-oxy-3-methoxy-phen-yl)propane-1, 3-diol threo-2-(2,6-Dimethoxy-phen-oxy)-1-(4-eth-oxy-3-methoxy-phen-yl)propane-1, 3-diol Acta Crystallographica Section E: Structure Reports Online, 65, 6, 1389-1390 Acta Crystallographica Section E: Structure Reports Online, 65, 6, 1389-1390 Acta Crystallographica Section E: Structure Reports Online, 65, 6, 1389-1390 2009 Refereed English Disclose to all
H. Tsuji, I. Tanaka, K. Endo, K.-I. Yamagata, M. Nakamura, E. Nakamura H. Tsuji, I. Tanaka, K. Endo, K.-I. Yamagata, M. Nakamura, E. Nakamura H. Tsuji, I. Tanaka, K. Endo, K.-I. Yamagata, M. Nakamura, E. Nakamura Indium-catalyzed [1 + n] annulation reaction between β-ketoester and αω-diyne Indium-catalyzed [1 + n] annulation reaction between β-ketoester and αω-diyne Indium-catalyzed [1 + n] annulation reaction between β-ketoester and αω-diyne Organic Letters, 11, 8, 1845-1847 Organic Letters, 11, 8, 1845-1847 Organic Letters, 11, 8, 1845-1847 2009 Refereed English Disclose to all
Noda, D., Sunada, Y., Hatakeyama, T., Nakamura, M., Nagashima, H. Noda, D., Sunada, Y., Hatakeyama, T., Nakamura, M., Nagashima, H. Noda, D., Sunada, Y., Hatakeyama, T., Nakamura, M., Nagashima, H. Effect of TMEDA on iron-catalyzed coupling reactions of ArMgX with alkyl halides Effect of TMEDA on iron-catalyzed coupling reactions of ArMgX with alkyl halides Effect of TMEDA on iron-catalyzed coupling reactions of ArMgX with alkyl halides Journal of the American Chemical Society, 131, 17, 6078-6079 Journal of the American Chemical Society, 131, 17, 6078-6079 Journal of the American Chemical Society, 131, 17, 6078-6079 2009 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Kondo, Y., Fujiwara, Y.-I., Takaya, H., Ito, S., Nakamura, E., Nakamura, M. Hatakeyama, T., Kondo, Y., Fujiwara, Y.-I., Takaya, H., Ito, S., Nakamura, E., Nakamura, M. Hatakeyama, T., Kondo, Y., Fujiwara, Y.-I., Takaya, H., Ito, S., Nakamura, E., Nakamura, M. Iron-catalysed fluoroaromatic coupling reactions under catalytic modulation with 1,2-bis(diphenylphosphino)benzene Iron-catalysed fluoroaromatic coupling reactions under catalytic modulation with 1,2-bis(diphenylphosphino)benzene Iron-catalysed fluoroaromatic coupling reactions under catalytic modulation with 1,2-bis(diphenylphosphino)benzene Chemical Communications, 10, 1216-1218 Chemical Communications, 10, 1216-1218 Chemical Communications, 10, 1216-1218 2009 Refereed English Research paper(scientific journal) Disclose to all
K. Yashio, M. Kawahata, H. Danjo, K. Yamaguchi, M. Nakamura, T. Imamoto K. Yashio, M. Kawahata, H. Danjo, K. Yamaguchi, M. Nakamura, T. Imamoto K. Yashio, M. Kawahata, H. Danjo, K. Yamaguchi, M. Nakamura, T. Imamoto Construction of optically active multimetallic systems of rhodium(I), palladium(II), and ruthenium(II) with a P-chiral tetraphosphine ligand Construction of optically active multimetallic systems of rhodium(I), palladium(II), and ruthenium(II) with a P-chiral tetraphosphine ligand Construction of optically active multimetallic systems of rhodium(I), palladium(II), and ruthenium(II) with a P-chiral tetraphosphine ligand Journal of Organometallic Chemistry, 694, 1, 97-102 Journal of Organometallic Chemistry, 694, 1, 97-102 Journal of Organometallic Chemistry, 694, 1, 97-102 2009 Refereed English Disclose to all
Hatakeyama, T., Hashimoto, S., Ishizuka, K., Nakamura, M. Hatakeyama, T., Hashimoto, S., Ishizuka, K., Nakamura, M. Hatakeyama, T., Hashimoto, S., Ishizuka, K., Nakamura, M. Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: A new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: A new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: A new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides Journal of the American Chemical Society, 131, 33, 11949-11963 Journal of the American Chemical Society, 131, 33, 11949-11963 Journal of the American Chemical Society, 131, 33, 11949-11963 2009 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Yoshimoto, Y., Gabriel, T., Nakamura, M. Hatakeyama, T., Yoshimoto, Y., Gabriel, T., Nakamura, M. Hatakeyama, T., Yoshimoto, Y., Gabriel, T., Nakamura, M. Iron-catalyzed enyne cross-coupling reaction Iron-catalyzed enyne cross-coupling reaction Iron-catalyzed enyne cross-coupling reaction Organic Letters, 10, 23, 5341-5344 Organic Letters, 10, 23, 5341-5344 Organic Letters, 10, 23, 5341-5344 2008 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Nakamura, M., Nakamura, E. Hatakeyama, T., Nakamura, M., Nakamura, E. Hatakeyama, T., Nakamura, M., Nakamura, E. Diastereoselective addition of zincated hydrazones to alkenylboronates and stereospecific trapping of boron/zinc bimetallic intermediates by carbon electrophiles Diastereoselective addition of zincated hydrazones to alkenylboronates and stereospecific trapping of boron/zinc bimetallic intermediates by carbon electrophiles Diastereoselective addition of zincated hydrazones to alkenylboronates and stereospecific trapping of boron/zinc bimetallic intermediates by carbon electrophiles Journal of the American Chemical Society, 130, 46, 15688-15701 Journal of the American Chemical Society, 130, 46, 15688-15701 Journal of the American Chemical Society, 130, 46, 15688-15701 2008 Refereed English Research paper(scientific journal) Disclose to all
Y. Itoh, H. Tsuji, K.-I. Yamagata, K. Endo, I. Tanaka, M. Nakamura, E. Nakamura Y. Itoh, H. Tsuji, K.-I. Yamagata, K. Endo, I. Tanaka, M. Nakamura, E. Nakamura Y. Itoh, H. Tsuji, K.-I. Yamagata, K. Endo, I. Tanaka, M. Nakamura, E. Nakamura Efficient formation of ring structures utilizing multisite activation by indium catalysis Efficient formation of ring structures utilizing multisite activation by indium catalysis Efficient formation of ring structures utilizing multisite activation by indium catalysis Journal of the American Chemical Society, 130, 50, 17161-17167 Journal of the American Chemical Society, 130, 50, 17161-17167 Journal of the American Chemical Society, 130, 50, 17161-17167 2008 Refereed English Disclose to all
H. Tsuji, T. Fujimoto, K. Endo, M. Nakamura, E. Nakamura H. Tsuji, T. Fujimoto, K. Endo, M. Nakamura, E. Nakamura H. Tsuji, T. Fujimoto, K. Endo, M. Nakamura, E. Nakamura Stereoselective synthesis of trisubstituted E-iodoalkenes by indium-catalyzed syn-addition of 1,3-dicarbonyi compounds to 1-iodoaikynes Stereoselective synthesis of trisubstituted E-iodoalkenes by indium-catalyzed syn-addition of 1,3-dicarbonyi compounds to 1-iodoaikynes Stereoselective synthesis of trisubstituted E-iodoalkenes by indium-catalyzed syn-addition of 1,3-dicarbonyi compounds to 1-iodoaikynes Organic Letters, 10, 6, 1219-1221 Organic Letters, 10, 6, 1219-1221 Organic Letters, 10, 6, 1219-1221 2008 Refereed English Disclose to all
T. Fujimoto, K. Endo, H. Tsuji, M. Nakamura, E. Nakamura T. Fujimoto, K. Endo, H. Tsuji, M. Nakamura, E. Nakamura T. Fujimoto, K. Endo, H. Tsuji, M. Nakamura, E. Nakamura Construction of a chiral quaternary carbon center by indium-catalyzed asymmetric α-alkenylation of β-ketoesters Construction of a chiral quaternary carbon center by indium-catalyzed asymmetric α-alkenylation of β-ketoesters Construction of a chiral quaternary carbon center by indium-catalyzed asymmetric α-alkenylation of β-ketoesters Journal of the American Chemical Society, 130, 13, 4492-4496 Journal of the American Chemical Society, 130, 13, 4492-4496 Journal of the American Chemical Society, 130, 13, 4492-4496 2008 Refereed English Disclose to all
Hatakeyama, T., Ito, S., Yamane, H., Nakamura, M., Nakamura, E. T. Hatakeyama, S. Ito, H. Yamane, M. Nakamura, E. Nakamura Hatakeyama, T., Ito, S., Yamane, H., Nakamura, M., Nakamura, E. Regioselective α-alkylation of ketones with alkyl chlorides and fluorides via highly nucleophilic magnesium enamides Regioselective α-alkylation of ketones with alkyl chlorides and fluorides via highly nucleophilic magnesium enamides Regioselective α-alkylation of ketones with alkyl chlorides and fluorides via highly nucleophilic magnesium enamides Tetrahedron, 63, 35, 8440-8448 Tetrahedron, 63, 35, 8440-8448 Tetrahedron, 63, 35, 8440-8448 2007 Refereed English Research paper(scientific journal) Disclose to all
Hatakeyama, T., Nakamura, M. Hatakeyama, T., Nakamura, M. Hatakeyama, T., Nakamura, M. Iron-catalyzed selective biaryl coupling: Remarkable suppression of homocoupling by the fluoride anion Iron-catalyzed selective biaryl coupling: Remarkable suppression of homocoupling by the fluoride anion Iron-catalyzed selective biaryl coupling: Remarkable suppression of homocoupling by the fluoride anion Journal of the American Chemical Society, 129, 32, 9844-9845 Journal of the American Chemical Society, 129, 32, 9844-9845 Journal of the American Chemical Society, 129, 32, 9844-9845 2007 Refereed English Research paper(scientific journal) Disclose to all
Endo, K., Hatakeyama, T., Nakamura, M., Nakamura, E. Endo, K., Hatakeyama, T., Nakamura, M., Nakamura, E. Endo, K., Hatakeyama, T., Nakamura, M., Nakamura, E. Indium-catalyzed 2-alkenylation of 1,3-dicarbonyl compounds with unactivated alkynes Indium-catalyzed 2-alkenylation of 1,3-dicarbonyl compounds with unactivated alkynes Indium-catalyzed 2-alkenylation of 1,3-dicarbonyl compounds with unactivated alkynes Journal of the American Chemical Society, 129, 16, 5264-5271 Journal of the American Chemical Society, 129, 16, 5264-5271 Journal of the American Chemical Society, 129, 16, 5264-5271 2007 Refereed English Research paper(scientific journal) Disclose to all
H. Tsuji, K.-I. Yamagata, Y. Itoh, K. Endo, M. Nakamura, E. Nakamura H. Tsuji, K.-I. Yamagata, Y. Itoh, K. Endo, M. Nakamura, E. Nakamura H. Tsuji, K.-I. Yamagata, Y. Itoh, K. Endo, M. Nakamura, E. Nakamura Indium-catalyzed cycloisomerization of ω-alkynyl-β-ketoesters into six- to fifteen-membered rings Indium-catalyzed cycloisomerization of ω-alkynyl-β-ketoesters into six- to fifteen-membered rings Indium-catalyzed cycloisomerization of ω-alkynyl-β-ketoesters into six- to fifteen-membered rings Angewandte Chemie - International Edition, 46, 42, 8060-8062 Angewandte Chemie - International Edition, 46, 42, 8060-8062 Angewandte Chemie - International Edition, 46, 42, 8060-8062 2007 Refereed English Disclose to all
M. Nakamura, L. Ilies, S. Otsubo, E. Nakamura M. Nakamura, L. Ilies, S. Otsubo, E. Nakamura M. Nakamura, L. Ilies, S. Otsubo, E. Nakamura 3-Zinciobenzofuran and 3-zincioindole: Versatile tools for the construction of conjugated structures containing multiple benzoheterole units 3-Zinciobenzofuran and 3-zincioindole: Versatile tools for the construction of conjugated structures containing multiple benzoheterole units 3-Zinciobenzofuran and 3-zincioindole: Versatile tools for the construction of conjugated structures containing multiple benzoheterole units Angewandte Chemie - International Edition, 45, 6, 944-947 Angewandte Chemie - International Edition, 45, 6, 944-947 Angewandte Chemie - International Edition, 45, 6, 944-947 2006 Refereed English Disclose to all
Nakamura, M, Ilies, L, Otsubo, S, Nakamura, E Nakamura, M, Ilies, L, Otsubo, S, Nakamura, E Nakamura, M, Ilies, L, Otsubo, S, Nakamura, E 2,3-Disubstituted Benzofuran and Indole by Copper-Mediated C?C Bond Extension Reaction of 3-Zinciobenzoheterole 2,3-Disubstituted Benzofuran and Indole by Copper-Mediated C?C Bond Extension Reaction of 3-Zinciobenzoheterole 2,3-Disubstituted Benzofuran and Indole by Copper-Mediated C?C Bond Extension Reaction of 3-Zinciobenzoheterole Org. Lett., 8, 13, 2803-2805 Org. Lett., 8, 13, 2803-2805 Org. Lett., 8, 13, 2803-2805 2006 Refereed English Disclose to all
M. Nakamura, S. Ito, K. Matsuo, E. Nakamura M. Nakamura, S. Ito, K. Matsuo, E. Nakamura M. Nakamura, S. Ito, K. Matsuo, E. Nakamura Iron-catalyzed chemoselective cross-coupling of primary and secondary alkyl halides with arylzinc reagents Iron-catalyzed chemoselective cross-coupling of primary and secondary alkyl halides with arylzinc reagents Iron-catalyzed chemoselective cross-coupling of primary and secondary alkyl halides with arylzinc reagents Synlett, 11, 1794-1798 Synlett, 11, 1794-1798 Synlett, 11, 1794-1798 2005/07 Refereed English Disclose to all
Hatakeyama, T., Ito, S., Nakamura, M., Nakamura, E. Hatakeyama, T., Ito, S., Nakamura, M., Nakamura, E. Hatakeyama, T., Ito, S., Nakamura, M., Nakamura, E. Alkylation of magnesium enamide with alkyl chlorides and fluorides Alkylation of magnesium enamide with alkyl chlorides and fluorides Alkylation of magnesium enamide with alkyl chlorides and fluorides Journal of the American Chemical Society, 127, 41, 14192-14193 Journal of the American Chemical Society, 127, 41, 14192-14193 Journal of the American Chemical Society, 127, 41, 14192-14193 2005 Refereed English Research paper(scientific journal) Disclose to all
M. Nakamura, A. Hajra, K. Endo, E. Nakamura M. Nakamura, A. Hajra, K. Endo, E. Nakamura M. Nakamura, A. Hajra, K. Endo, E. Nakamura Synthesis of chiral α-fluoroketones through catalytic enantioselective decarboxylation Synthesis of chiral α-fluoroketones through catalytic enantioselective decarboxylation Synthesis of chiral α-fluoroketones through catalytic enantioselective decarboxylation Angewandte Chemie - International Edition, 44, 44, 7248-7251 Angewandte Chemie - International Edition, 44, 44, 7248-7251 Angewandte Chemie - International Edition, 44, 44, 7248-7251 2005 Refereed English Disclose to all
M. Nakamura, K. Endo, E. Nakamura M. Nakamura, K. Endo, E. Nakamura M. Nakamura, K. Endo, E. Nakamura A modular approach to α-arylated carbonyl compounds via indium tris(bistriflylamide)-catalyzed regioselective addition of β-ketoesters to 1,3-diynes A modular approach to α-arylated carbonyl compounds via indium tris(bistriflylamide)-catalyzed regioselective addition of β-ketoesters to 1,3-diynes A modular approach to α-arylated carbonyl compounds via indium tris(bistriflylamide)-catalyzed regioselective addition of β-ketoesters to 1,3-diynes Advanced Synthesis and Catalysis, 347, 11/13, 1681-1686 Advanced Synthesis and Catalysis, 347, 11/13, 1681-1686 Advanced Synthesis and Catalysis, 347, 11/13, 1681-1686 2005 Refereed English Disclose to all
M. Nakamura, K. Endo, E. Nakamura M. Nakamura, K. Endo, E. Nakamura M. Nakamura, K. Endo, E. Nakamura Indium triflate-catalyzed vinylation of β-ketoesters with acetylene gas Indium triflate-catalyzed vinylation of β-ketoesters with acetylene gas Indium triflate-catalyzed vinylation of β-ketoesters with acetylene gas Organic Letters, 7, 15, 3279-3281 Organic Letters, 7, 15, 3279-3281 Organic Letters, 7, 15, 3279-3281 2005 Refereed English Disclose to all
M. Nakamura, K. Matsuo, S. Ito, E. Nakamura M. Nakamura, K. Matsuo, S. Ito, E. Nakamura M. Nakamura, K. Matsuo, S. Ito, E. Nakamura Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents Journal of the American Chemical Society, 126, 12, 3686-3687 Journal of the American Chemical Society, 126, 12, 3686-3687 Journal of the American Chemical Society, 126, 12, 3686-3687 2004/03 Refereed English Disclose to all
Nakamura, M., Hatakeyama, T., Hara, K., Fukudome, H., Nakamura, E. Nakamura, M., Hatakeyama, T., Hara, K., Fukudome, H., Nakamura, E. Nakamura, M., Hatakeyama, T., Hara, K., Fukudome, H., Nakamura, E. Sequential coupling of zincated hydrazone, alkenylboronate, and electrophile that creates several contiguous stereogenic centers Sequential coupling of zincated hydrazone, alkenylboronate, and electrophile that creates several contiguous stereogenic centers Sequential coupling of zincated hydrazone, alkenylboronate, and electrophile that creates several contiguous stereogenic centers Journal of the American Chemical Society, 126, 44, 14344-14345 Journal of the American Chemical Society, 126, 44, 14344-14345 Journal of the American Chemical Society, 126, 44, 14344-14345 2004 Refereed English Research paper(scientific journal) Disclose to all
Nakamura, M., Hatakeyama, T., Nakamura, E. M. Nakamura, T. Hatakeyama, E. Nakamura Nakamura, M., Hatakeyama, T., Nakamura, E. α-alkylation of ketones by addition of zinc enamides to unactivated olefins α-alkylation of ketones by addition of zinc enamides to unactivated olefins α-alkylation of ketones by addition of zinc enamides to unactivated olefins Journal of the American Chemical Society, 126, 38, 11820-11825 Journal of the American Chemical Society, 126, 38, 11820-11825 Journal of the American Chemical Society, 126, 38, 11820-11825 2004 Refereed English Research paper(scientific journal) Disclose to all
M. Uchiyama, S. Nakamura, T. Ohwada, M. Nakamura, E. Nakamura M. Uchiyama, S. Nakamura, T. Ohwada, M. Nakamura, E. Nakamura M. Uchiyama, S. Nakamura, T. Ohwada, M. Nakamura, E. Nakamura Mechanism and ligand-transfer selectivity of 1,2-addition of organozincate complexes to aldehyde Mechanism and ligand-transfer selectivity of 1,2-addition of organozincate complexes to aldehyde Mechanism and ligand-transfer selectivity of 1,2-addition of organozincate complexes to aldehyde Journal of the American Chemical Society, 126, 35, 10897-10903 Journal of the American Chemical Society, 126, 35, 10897-10903 Journal of the American Chemical Society, 126, 35, 10897-10903 2004 Refereed English Disclose to all
M. Nakamura, C. Liang, E. Nakamura M. Nakamura, C. Liang, E. Nakamura M. Nakamura, C. Liang, E. Nakamura Zn(II)/amine-catalyzed coupling reaction of alkylidenemalonates with propargyl alcohol: A one-pot synthesis of methylenetetrahydrofurans Zn(II)/amine-catalyzed coupling reaction of alkylidenemalonates with propargyl alcohol: A one-pot synthesis of methylenetetrahydrofurans Zn(II)/amine-catalyzed coupling reaction of alkylidenemalonates with propargyl alcohol: A one-pot synthesis of methylenetetrahydrofurans Organic Letters, 6, 12, 2015-2017 Organic Letters, 6, 12, 2015-2017 Organic Letters, 6, 12, 2015-2017 2004 Refereed English Disclose to all
M. Nakamura, T. Fujimoto, K. Endo, E. Nakamura M. Nakamura, T. Fujimoto, K. Endo, E. Nakamura M. Nakamura, T. Fujimoto, K. Endo, E. Nakamura Stereoselective synthesis of tetra-substituted olefins via addition of zinc enolates to unactivated alkynes Stereoselective synthesis of tetra-substituted olefins via addition of zinc enolates to unactivated alkynes Stereoselective synthesis of tetra-substituted olefins via addition of zinc enolates to unactivated alkynes Organic Letters, 6, 26, 4837-4840 Organic Letters, 6, 26, 4837-4840 Organic Letters, 6, 26, 4837-4840 2004 Refereed English Disclose to all
M. Nakamura, K. Matsuo, T. Inoue, E. Nakamura M. Nakamura, K. Matsuo, T. Inoue, E. Nakamura M. Nakamura, K. Matsuo, T. Inoue, E. Nakamura Iron-catalyzed regio- and stereoselective ring opening of [2.2.1]-and [3.2.1]oxabicyclic alkenes with a Grignard reagent Iron-catalyzed regio- and stereoselective ring opening of [2.2.1]-and [3.2.1]oxabicyclic alkenes with a Grignard reagent Iron-catalyzed regio- and stereoselective ring opening of [2.2.1]-and [3.2.1]oxabicyclic alkenes with a Grignard reagent Organic Letters, 5, 8, 1373-1375 Organic Letters, 5, 8, 1373-1375 Organic Letters, 5, 8, 1373-1375 2003/04 Refereed English Disclose to all
Nakamura, M., Hatakeyama, T., Hara, K., Nakamura, E. M. Nakamura, T. Hatakeyama, K. Hara, E. Nakamura Nakamura, M., Hatakeyama, T., Hara, K., Nakamura, E. Enantioselective synthesis of α-substituted ketones by asymmetric addition of chiral zinc enamides to 1-alkenes Enantioselective synthesis of α-substituted ketones by asymmetric addition of chiral zinc enamides to 1-alkenes Enantioselective synthesis of α-substituted ketones by asymmetric addition of chiral zinc enamides to 1-alkenes Journal of the American Chemical Society, 125, 21, 6362-6363 Journal of the American Chemical Society, 125, 21, 6362-6363 Journal of the American Chemical Society, 125, 21, 6362-6363 2003 Refereed English Research paper(scientific journal) Disclose to all
M. Nakamura, K. Endo, E. Nakamura M. Nakamura, K. Endo, E. Nakamura M. Nakamura, K. Endo, E. Nakamura Indium-Catalyzed Addition of Active Methylene Compounds to 1-Alkynes Indium-Catalyzed Addition of Active Methylene Compounds to 1-Alkynes Indium-Catalyzed Addition of Active Methylene Compounds to 1-Alkynes Journal of the American Chemical Society, 125, 43, 13002-13003 Journal of the American Chemical Society, 125, 43, 13002-13003 Journal of the American Chemical Society, 125, 43, 13002-13003 2003 Refereed English Disclose to all
M. Nakamura, A. Hirai, E. Nakamura M. Nakamura, A. Hirai, E. Nakamura M. Nakamura, A. Hirai, E. Nakamura Reaction pathways of the Simmons-Smith reaction Reaction pathways of the Simmons-Smith reaction Reaction pathways of the Simmons-Smith reaction Journal of the American Chemical Society, 125, 8, 2341-2350 Journal of the American Chemical Society, 125, 8, 2341-2350 Journal of the American Chemical Society, 125, 8, 2341-2350 2003 Refereed English Disclose to all
Nakamura, M, Wang, X.-Q, Isaka, M, Yamago, S, Nakamura, E Nakamura, M, Wang, X.-Q, Isaka, M, Yamago, S, Nakamura, E Nakamura, M, Wang, X.-Q, Isaka, M, Yamago, S, Nakamura, E Synthesis and [3+2] Cycloaddition of 2,2-Dialkoxy-1-methylenecyclopropane: 6,6-Dimethyl-1-methylene- 4,8-dioxaspiro[2.5]octane Synthesis and [3+2] Cycloaddition of 2,2-Dialkoxy-1-methylenecyclopropane: 6,6-Dimethyl-1-methylene- 4,8-dioxaspiro[2.5]octane Synthesis and [3+2] Cycloaddition of 2,2-Dialkoxy-1-methylenecyclopropane: 6,6-Dimethyl-1-methylene- 4,8-dioxaspiro[2.5]octane Org. Synth., 80, 144-159 Org. Synth., 80, 144-159 Org. Synth., 80, 144-159 2003 Refereed English Disclose to all
M. Nakamura, N. Yoshikai, E. Nakamura M. Nakamura, N. Yoshikai, E. Nakamura M. Nakamura, N. Yoshikai, E. Nakamura Carbozincation of dipolar trimethylenemethane. A new route to functionalized organozinc reagents Carbozincation of dipolar trimethylenemethane. A new route to functionalized organozinc reagents Carbozincation of dipolar trimethylenemethane. A new route to functionalized organozinc reagents Chemistry Letters, 2, 146-147 Chemistry Letters, 2, 146-147 Chemistry Letters, 2, 146-147 2002 Refereed English Disclose to all
Nakamura, M., Hara, K., Hatakeyama, T., Nakamura, E. Nakamura, M., Hara, K., Hatakeyama, T., Nakamura, E. Nakamura, M., Hara, K., Hatakeyama, T., Nakamura, E. Regioselective allylzincation of alkenylboronate Regioselective allylzincation of alkenylboronate Regioselective allylzincation of alkenylboronate Organic Letters, 3, 20, 3137-3140 Organic Letters, 3, 20, 3137-3140 Organic Letters, 3, 20, 3137-3140 2001 Refereed English Research paper(scientific journal) Disclose to all
H. Ohara, T. Itoh, M. Nakamura, E. Nakamura H. Ohara, T. Itoh, M. Nakamura, E. Nakamura H. Ohara, T. Itoh, M. Nakamura, E. Nakamura [2+2]-cycloaddition reaction of styrene derivatives using an Fe(III) salt catalyst [2+2]-cycloaddition reaction of styrene derivatives using an Fe(III) salt catalyst [2+2]-cycloaddition reaction of styrene derivatives using an Fe(III) salt catalyst Chemistry Letters, 7, 624-625 Chemistry Letters, 7, 624-625 Chemistry Letters, 7, 624-625 2001 Refereed English Disclose to all
M. Nakamura, N. Yoshikai, M. Toganoh, E. Nakamura M. Nakamura, N. Yoshikai, M. Toganoh, E. Nakamura M. Nakamura, N. Yoshikai, M. Toganoh, E. Nakamura [3+3] cycloaddition reaction of dipolar trimethylenemethane with active methylene compound [3+3] cycloaddition reaction of dipolar trimethylenemethane with active methylene compound [3+3] cycloaddition reaction of dipolar trimethylenemethane with active methylene compound Synlett, SPEC. ISS, 1030-1033 Synlett, SPEC. ISS, 1030-1033 Synlett, SPEC. ISS, 1030-1033 2001 Refereed English Disclose to all
M. Nakamura, T. Inoue, E. Nakamura M. Nakamura, T. Inoue, E. Nakamura M. Nakamura, T. Inoue, E. Nakamura Synthesis of substituted cyclopropanone acetals by carbometallation and its oxidative cleavage with manganese(IV) oxide and lead(IV) oxide Synthesis of substituted cyclopropanone acetals by carbometallation and its oxidative cleavage with manganese(IV) oxide and lead(IV) oxide Synthesis of substituted cyclopropanone acetals by carbometallation and its oxidative cleavage with manganese(IV) oxide and lead(IV) oxide Journal of Organometallic Chemistry, 624, 1/2, 300-306 Journal of Organometallic Chemistry, 624, 1/2, 300-306 Journal of Organometallic Chemistry, 624, 1/2, 300-306 2001 Refereed English Disclose to all
M. Nakamura, A. Hirai, E. Nakamura M. Nakamura, A. Hirai, E. Nakamura M. Nakamura, A. Hirai, E. Nakamura Iron-catalyzed olefin carbometalation [15] Iron-catalyzed olefin carbometalation [15] Iron-catalyzed olefin carbometalation [15] Journal of the American Chemical Society, 122, 5, 978-979 Journal of the American Chemical Society, 122, 5, 978-979 Journal of the American Chemical Society, 122, 5, 978-979 2000/02 Refereed English Disclose to all
M. Nakamura, M. Toganoh, X.Q. Wang, S. Yamago, E. Nakamura M. Nakamura, M. Toganoh, X.Q. Wang, S. Yamago, E. Nakamura M. Nakamura, M. Toganoh, X.Q. Wang, S. Yamago, E. Nakamura Intramolecular [3 + 2]cycloaddition reaction of dipolar trimethylenemethane Intramolecular [3 + 2]cycloaddition reaction of dipolar trimethylenemethane Intramolecular [3 + 2]cycloaddition reaction of dipolar trimethylenemethane Chemistry Letters, 6, 664-665 Chemistry Letters, 6, 664-665 Chemistry Letters, 6, 664-665 2000 Refereed English Disclose to all
H. Ohara, K. Kudo, T. Itoh, M. Nakamura, E. Nakamura H. Ohara, K. Kudo, T. Itoh, M. Nakamura, E. Nakamura H. Ohara, K. Kudo, T. Itoh, M. Nakamura, E. Nakamura Fe(III)-catalyzed radical cyclization of cyclopropanone thioacetal Fe(III)-catalyzed radical cyclization of cyclopropanone thioacetal Fe(III)-catalyzed radical cyclization of cyclopropanone thioacetal Heterocycles, 52, 2, 505-510 Heterocycles, 52, 2, 505-510 Heterocycles, 52, 2, 505-510 2000 Refereed English Disclose to all
S. Mori, A. Hirai, M. Nakamura, E. Nakamura S. Mori, A. Hirai, M. Nakamura, E. Nakamura S. Mori, A. Hirai, M. Nakamura, E. Nakamura Correlation of reactivities of organocuprate(I) and zincate(II) with d- orbital energies of ate complexes Correlation of reactivities of organocuprate(I) and zincate(II) with d- orbital energies of ate complexes Correlation of reactivities of organocuprate(I) and zincate(II) with d- orbital energies of ate complexes Tetrahedron, 56, 18, 2805-2809 Tetrahedron, 56, 18, 2805-2809 Tetrahedron, 56, 18, 2805-2809 2000 Refereed English Disclose to all
A. Hirai, M. Nakamura, E. Nakamura A. Hirai, M. Nakamura, E. Nakamura A. Hirai, M. Nakamura, E. Nakamura Mechanism of addition of allylmetal to vinylmetal. Dichotomy between metallo-ene reaction and metalla-Claisen rearrangement Mechanism of addition of allylmetal to vinylmetal. Dichotomy between metallo-ene reaction and metalla-Claisen rearrangement Mechanism of addition of allylmetal to vinylmetal. Dichotomy between metallo-ene reaction and metalla-Claisen rearrangement Journal of the American Chemical Society, 122, 48, 11791-11798 Journal of the American Chemical Society, 122, 48, 11791-11798 Journal of the American Chemical Society, 122, 48, 11791-11798 2000 Refereed English Disclose to all
M. Nakamura, T. Inoue, A. Sato, E. Nakamura M. Nakamura, T. Inoue, A. Sato, E. Nakamura M. Nakamura, T. Inoue, A. Sato, E. Nakamura Asymmetric construction of quaternary carbon centers by regio- and enantiocontrolled allylzincation Asymmetric construction of quaternary carbon centers by regio- and enantiocontrolled allylzincation Asymmetric construction of quaternary carbon centers by regio- and enantiocontrolled allylzincation Organic Letters, 2, 15, 2193-2196 Organic Letters, 2, 15, 2193-2196 Organic Letters, 2, 15, 2193-2196 2000 Refereed English Disclose to all
A. Hirai, M. Nakamura, E. Nakamura A. Hirai, M. Nakamura, E. Nakamura A. Hirai, M. Nakamura, E. Nakamura Synergetic dimetallic effects in Gaudemar/Normant coupling between allylzinc and vinyl grignard reagents [11] Synergetic dimetallic effects in Gaudemar/Normant coupling between allylzinc and vinyl grignard reagents [11] Synergetic dimetallic effects in Gaudemar/Normant coupling between allylzinc and vinyl grignard reagents [11] Journal of the American Chemical Society, 121, 37, 8665-8666 Journal of the American Chemical Society, 121, 37, 8665-8666 Journal of the American Chemical Society, 121, 37, 8665-8666 1999 Refereed English Disclose to all
M. Nakamura, M. Toganoh, H. Ohara, E. Nakamura M. Nakamura, M. Toganoh, H. Ohara, E. Nakamura M. Nakamura, M. Toganoh, H. Ohara, E. Nakamura Cycloaddition reactions of trimethylenemethane radical cation generated from methylenecyclopropanone thioacetal Cycloaddition reactions of trimethylenemethane radical cation generated from methylenecyclopropanone thioacetal Cycloaddition reactions of trimethylenemethane radical cation generated from methylenecyclopropanone thioacetal Organic Letters, 1, 1, 7-9 Organic Letters, 1, 1, 7-9 Organic Letters, 1, 1, 7-9 1999 Refereed English Disclose to all
M. Nakamura, K. Hara, G. Sakata, E. Nakamura M. Nakamura, K. Hara, G. Sakata, E. Nakamura M. Nakamura, K. Hara, G. Sakata, E. Nakamura One-pot synthesis of pyrroles through carbometalation reaction of zincated hydrazone with vinylstannane One-pot synthesis of pyrroles through carbometalation reaction of zincated hydrazone with vinylstannane One-pot synthesis of pyrroles through carbometalation reaction of zincated hydrazone with vinylstannane Organic Letters, 1, 10, 1505-1507 Organic Letters, 1, 10, 1505-1507 Organic Letters, 1, 10, 1505-1507 1999 Refereed English Disclose to all
S. Yamago, M. Nakamura, X.Q. Wang, M. Yanagawa, S. Tokumitsu, E. Nakamura S. Yamago, M. Nakamura, X.Q. Wang, M. Yanagawa, S. Tokumitsu, E. Nakamura S. Yamago, M. Nakamura, X.Q. Wang, M. Yanagawa, S. Tokumitsu, E. Nakamura Thermal Hetero [3 + 2] Cycloaddition of Dipolar Trimethylenemethane to O-Alkyloximes. Straightforward Synthetic Routes to Substituted Pyrrolidines and Prolines Thermal Hetero [3 + 2] Cycloaddition of Dipolar Trimethylenemethane to O-Alkyloximes. Straightforward Synthetic Routes to Substituted Pyrrolidines and Prolines Thermal Hetero [3 + 2] Cycloaddition of Dipolar Trimethylenemethane to O-Alkyloximes. Straightforward Synthetic Routes to Substituted Pyrrolidines and Prolines Journal of Organic Chemistry, 63, 5, 1694-1703 Journal of Organic Chemistry, 63, 5, 1694-1703 Journal of Organic Chemistry, 63, 5, 1694-1703 1998/03 Refereed English Disclose to all
A. Hirai, M. Nakamura, E. Nakamura A. Hirai, M. Nakamura, E. Nakamura A. Hirai, M. Nakamura, E. Nakamura Theoretical studies on cyclopropanation reaction with lithium and zinc carbenoids Theoretical studies on cyclopropanation reaction with lithium and zinc carbenoids Theoretical studies on cyclopropanation reaction with lithium and zinc carbenoids Chemistry Letters, 9, 927-928 Chemistry Letters, 9, 927-928 Chemistry Letters, 9, 927-928 1998 Refereed English Disclose to all
K. Kubota, S. Mori, M. Nakamura, E. Nakamura K. Kubota, S. Mori, M. Nakamura, E. Nakamura K. Kubota, S. Mori, M. Nakamura, E. Nakamura Olefin carbometalation with (Alkoxy)allylic lithium and zinc reagents. Four-centered vs six-centered mechanism of allylmetalation reaction Olefin carbometalation with (Alkoxy)allylic lithium and zinc reagents. Four-centered vs six-centered mechanism of allylmetalation reaction Olefin carbometalation with (Alkoxy)allylic lithium and zinc reagents. Four-centered vs six-centered mechanism of allylmetalation reaction Journal of the American Chemical Society, 120, 51, 13334-13341 Journal of the American Chemical Society, 120, 51, 13334-13341 Journal of the American Chemical Society, 120, 51, 13334-13341 1998 Refereed English Disclose to all
E. Nakamura, A. Hirai, M. Nakamura E. Nakamura, A. Hirai, M. Nakamura E. Nakamura, A. Hirai, M. Nakamura Theoretical studies on lewis acid acceleration in Simmons-Smith reaction [20] Theoretical studies on lewis acid acceleration in Simmons-Smith reaction [20] Theoretical studies on lewis acid acceleration in Simmons-Smith reaction [20] Journal of the American Chemical Society, 120, 23, 5844-5845 Journal of the American Chemical Society, 120, 23, 5844-5845 Journal of the American Chemical Society, 120, 23, 5844-5845 1998 Refereed English Disclose to all
M. Nakamura, A. Hirai, M. Sogi, E. Nakamura M. Nakamura, A. Hirai, M. Sogi, E. Nakamura M. Nakamura, A. Hirai, M. Sogi, E. Nakamura Enantioselective addition of allylzinc reagent to alkynyl ketones [21] Enantioselective addition of allylzinc reagent to alkynyl ketones [21] Enantioselective addition of allylzinc reagent to alkynyl ketones [21] Journal of the American Chemical Society, 120, 23, 5846-5847 Journal of the American Chemical Society, 120, 23, 5846-5847 Journal of the American Chemical Society, 120, 23, 5846-5847 1998 Refereed English Disclose to all
M. Nakamura, E. Nakamura M. Nakamura, E. Nakamura M. Nakamura, E. Nakamura Preparative Routes to Organozinc Reagents Used for Organic Synthesis Preparative Routes to Organozinc Reagents Used for Organic Synthesis Preparative Routes to Organozinc Reagents Used for Organic Synthesis Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 56, 8, 632-644 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 56, 8, 632-644 Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry, 56, 8, 632-644 1998 Refereed English Disclose to all
S. Mori, B.H. Kim, M. Nakamura, E. Nakamura S. Mori, B.H. Kim, M. Nakamura, E. Nakamura S. Mori, B.H. Kim, M. Nakamura, E. Nakamura Open dimer participation in chelation controlled addition of methyllithium dimer to α-and β-alkoxy aldehydes Open dimer participation in chelation controlled addition of methyllithium dimer to α-and β-alkoxy aldehydes Open dimer participation in chelation controlled addition of methyllithium dimer to α-and β-alkoxy aldehydes Chemistry Letters, 10, 1079-1080 Chemistry Letters, 10, 1079-1080 Chemistry Letters, 10, 1079-1080 1997 Refereed English Disclose to all
E. Nakamura, S. Mori, M. Nakamura, K. Morokuma E. Nakamura, S. Mori, M. Nakamura, K. Morokuma E. Nakamura, S. Mori, M. Nakamura, K. Morokuma Theoretical studies on the addition of polymetallic lithium organocuprate clusters to acetylene. Cooperative effects of metals in a trap-and-bite reaction pathway Theoretical studies on the addition of polymetallic lithium organocuprate clusters to acetylene. Cooperative effects of metals in a trap-and-bite reaction pathway Theoretical studies on the addition of polymetallic lithium organocuprate clusters to acetylene. Cooperative effects of metals in a trap-and-bite reaction pathway Journal of the American Chemical Society, 119, 21, 4887-4899 Journal of the American Chemical Society, 119, 21, 4887-4899 Journal of the American Chemical Society, 119, 21, 4887-4899 1997 Refereed English Disclose to all
H.Zushi, Y,Suzuki, M.Hosotubo, Y.Nakamura, M.Wakatani, F.Sano, K.Kondo, T.Mizuuchi, M.Nakasuga, S.Besshou, H.Okada, K.Nagasaki, C.Christou, Y.Kurimoto, H.Funaba, T.Hamada, T.Kinosita, T.Obiki, S.Kado, K.Muraoka, S.Sudo, K.Ida, B.J.Peterson, V.Yu.Sergeev, K.V.Khlopenkov, V.V.Chechkin, V.S.Voitsenya H.Zushi, Y,Suzuki, M.Hosotubo, Y.Nakamura, M.Wakatani, F.Sano, K.Kondo, T.Mizuuchi, M.Nakasuga, S.Besshou, H.Okada, K.Nagasaki, C.Christou, Y.Kurimoto, H.Funaba, T.Hamada, T.Kinosita, T.Obiki, S.Kado, K.Muraoka, S.Sudo, K.Ida, B.J.Peterson, V.Yu.Sergeev, K.V.Khlopenkov, V.V.Chechkin, V.S.Voitsenya H.Zushi, Y,Suzuki, M.Hosotubo, Y.Nakamura, M.Wakatani, F.Sano, K.Kondo, T.Mizuuchi, M.Nakasuga, S.Besshou, H.Okada, K.Nagasaki, C.Christou, Y.Kurimoto, H.Funaba, T.Hamada, T.Kinosita, T.Obiki, S.Kado, K.Muraoka, S.Sudo, K.Ida, B.J.Peterson, V.Yu.Sergeev, K.V.Khlopenkov, V.V.Chechkin, V.S.Voitsenya Resistive Effects on the Critical Pressure Gradient for the Resistive Interchange Modes in Heliotron-E Resistive Effects on the Critical Pressure Gradient for the Resistive Interchange Modes in Heliotron-E Resistive Effects on the Critical Pressure Gradient for the Resistive Interchange Modes in Heliotron-E IAE Research Report, No.16(1996) AE Research Report, No.16(1996) IAE Research Report, No.16(1996) 1996 Refereed English Disclose to all
Nakamura, M, Hirai, A, Nakamura, E Nakamura, M, Hirai, A, Nakamura, E Nakamura, M, Hirai, A, Nakamura, E Enantioselective Allylzincation of Cyclic Aldimines in the Presence of Anionic Bis-oxazoline Ligand Enantioselective Allylzincation of Cyclic Aldimines in the Presence of Anionic Bis-oxazoline Ligand Enantioselective Allylzincation of Cyclic Aldimines in the Presence of Anionic Bis-oxazoline Ligand J. Am. Chem. Soc., 118, 35, 8489-8490 J. Am. Chem. Soc., 118, 35, 8489-8490 J. Am. Chem. Soc., 118, 35, 8489-8490 1996 Refereed English Disclose to all
S. Mori, M. Nakamura, E. Nakamura, N. Koga, K. Morokuma S. Mori, M. Nakamura, E. Nakamura, N. Koga, K. Morokuma S. Mori, M. Nakamura, E. Nakamura, N. Koga, K. Morokuma Theoretical studies on chelation-controlled carbonyl addition. Me<sub>2</sub>Mg addition to α- and β-alkoxy ketones and aldehydes Theoretical studies on chelation-controlled carbonyl addition. Me<sub>2</sub>Mg addition to α- and β-alkoxy ketones and aldehydes Theoretical studies on chelation-controlled carbonyl addition. Me<sub>2</sub>Mg addition to α- and β-alkoxy ketones and aldehydes Journal of the American Chemical Society, 117, 18, 5055-5065 Journal of the American Chemical Society, 117, 18, 5055-5065 Journal of the American Chemical Society, 117, 18, 5055-5065 1995 Refereed English Disclose to all
M. Nakamura, M. Arai, E. Nakamura M. Nakamura, M. Arai, E. Nakamura M. Nakamura, M. Arai, E. Nakamura Carbometalation of cyclopropene. Ligand-induced enantioselective allylzincation Carbometalation of cyclopropene. Ligand-induced enantioselective allylzincation Carbometalation of cyclopropene. Ligand-induced enantioselective allylzincation Journal of the American Chemical Society, 117, 3, 1179-1180 Journal of the American Chemical Society, 117, 3, 1179-1180 Journal of the American Chemical Society, 117, 3, 1179-1180 1995 Refereed English Disclose to all
M. Nakamura, E. Nakamura, N. Koga, K. Morokuma M. Nakamura, E. Nakamura, N. Koga, K. Morokuma M. Nakamura, E. Nakamura, N. Koga, K. Morokuma Theoretical studies of nucleophilic additions of monomeric and dimeric organometallics Theoretical studies of nucleophilic additions of monomeric and dimeric organometallics Theoretical studies of nucleophilic additions of monomeric and dimeric organometallics Journal of the Chemical Society, Faraday Transactions, 90, 12, 1789-1798 Journal of the Chemical Society, Faraday Transactions, 90, 12, 1789-1798 Journal of the Chemical Society, Faraday Transactions, 90, 12, 1789-1798 1994 Refereed English Disclose to all
S. Yamago, S. Ejiri, M. Nakamura, E. Nakamura S. Yamago, S. Ejiri, M. Nakamura, E. Nakamura S. Yamago, S. Ejiri, M. Nakamura, E. Nakamura Single electron transfer pathway in the [3 + 2] cycloaddition of dipolar trimethylenemethane with otefins Single electron transfer pathway in the [3 + 2] cycloaddition of dipolar trimethylenemethane with otefins Single electron transfer pathway in the [3 + 2] cycloaddition of dipolar trimethylenemethane with otefins Journal of the American Chemical Society, 115, 12, 5344-5345 Journal of the American Chemical Society, 115, 12, 5344-5345 Journal of the American Chemical Society, 115, 12, 5344-5345 1993/06 Refereed English Disclose to all
H. Tokuyama, M. Nakamura, E. Nakamura H. Tokuyama, M. Nakamura, E. Nakamura H. Tokuyama, M. Nakamura, E. Nakamura [1 + 2] and [3 + 2] cycloaddition reactions of vinylcarbenes with C<sub>60</sub> [1 + 2] and [3 + 2] cycloaddition reactions of vinylcarbenes with C<sub>60</sub> [1 + 2] and [3 + 2] cycloaddition reactions of vinylcarbenes with C<sub>60</sub> Tetrahedron Letters, 34, 46, 7429-7432 Tetrahedron Letters, 34, 46, 7429-7432 Tetrahedron Letters, 34, 46, 7429-7432 1993 Refereed English Disclose to all
E. Nakamura, M. Nakamura, Y. Miyachi, N. Koga, K. Morokuma E. Nakamura, M. Nakamura, Y. Miyachi, N. Koga, K. Morokuma E. Nakamura, M. Nakamura, Y. Miyachi, N. Koga, K. Morokuma Theoretical studies on carbometalation of cyclopropene. Transition structures of addition of Me<sup>-</sup>, MeLi, MeCu, and Me<sub>2</sub>Cu<sup>-</sup> and origin of the high reactivity of the strained double bond Theoretical studies on carbometalation of cyclopropene. Transition structures of addition of Me<sup>-</sup>, MeLi, MeCu, and Me<sub>2</sub>Cu<sup>-</sup> and origin of the high reactivity of the strained double bond Theoretical studies on carbometalation of cyclopropene. Transition structures of addition of Me<sup>-</sup>, MeLi, MeCu, and Me<sub>2</sub>Cu<sup>-</sup> and origin of the high reactivity of the strained double bond Journal of the American Chemical Society, 115, 1, 99-106 Journal of the American Chemical Society, 115, 1, 99-106 Journal of the American Chemical Society, 115, 1, 99-106 1993 Refereed English Disclose to all
K. Kubota, M. Nakamura, M. Isaka, E. Nakamura K. Kubota, M. Nakamura, M. Isaka, E. Nakamura K. Kubota, M. Nakamura, M. Isaka, E. Nakamura Ligand control in the stereoselective allylzincation of cyclopropenes Ligand control in the stereoselective allylzincation of cyclopropenes Ligand control in the stereoselective allylzincation of cyclopropenes Journal of the American Chemical Society, 115, 13, 5867-5868 Journal of the American Chemical Society, 115, 13, 5867-5868 Journal of the American Chemical Society, 115, 13, 5867-5868 1993 Refereed English Disclose to all
M. Nakamura, E. Nakamura, N. Koga, K. Morokuma M. Nakamura, E. Nakamura, N. Koga, K. Morokuma M. Nakamura, E. Nakamura, N. Koga, K. Morokuma Theoretical studies on the reaction of solvated methyllithium open dimer with aldehyde Theoretical studies on the reaction of solvated methyllithium open dimer with aldehyde Theoretical studies on the reaction of solvated methyllithium open dimer with aldehyde Journal of the American Chemical Society, 115, 23, 11016-11017 Journal of the American Chemical Society, 115, 23, 11016-11017 Journal of the American Chemical Society, 115, 23, 11016-11017 1993 Refereed English Disclose to all
NAKAMURA Masaharu 中村 正治 NAKAMURA Masaharu Iron-catalyzed Alkyl–Alkyl Negishi Coupling of Organoaluminum Reagents Iron-catalyzed Alkyl–Alkyl Negishi Coupling of Organoaluminum Reagents Iron-catalyzed Alkyl–Alkyl Negishi Coupling of Organoaluminum Reagents Chem. Lett., 48, 238-241 Chem. Lett., 48, 238-241 Chem. Lett., 48, 238-241 Refereed Disclose to all

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Title language:
Misc
Author Author(Japanese) Author(English) Title Title(Japanese) Title(English) Bibliography Bibliography(Japanese) Bibliography(English) Publication date Refereed paper Language Publishing type Disclose
Nakamura, E, Hatakeyama, T, Ito, S, Ishizuka, K, Ilies, L, Nakamura, M Nakamura, E, Hatakeyama, T, Ito, S, Ishizuka, K, Ilies, L, Nakamura, M Nakamura, E, Hatakeyama, T, Ito, S, Ishizuka, K, Ilies, L, Nakamura, M Iron-Catalyzed Cross-Coupling Reactions Iron-Catalyzed Cross-Coupling Reactions Iron-Catalyzed Cross-Coupling Reactions Org. React., 83, 1-209 Org. React., 83, 1-209 Org. React., 83, 1-209 2014 English Disclose to all
Hatakeyama, T, Ishizuka, K, Nakamura, M Hatakeyama, T, Ishizuka, K, Nakamura, M Hatakeyama, T, Ishizuka, K, Nakamura, M Cross-Coupling Reactions Catalyzed by Iron Group Metals and N-Heterocyclic Carbenes via Nonconventional Reaction Mechanisms Cross-Coupling Reactions Catalyzed by Iron Group Metals and N-Heterocyclic Carbenes via Nonconventional Reaction Mechanisms Cross-Coupling Reactions Catalyzed by Iron Group Metals and N-Heterocyclic Carbenes via Nonconventional Reaction Mechanisms J. Synth. Org., Chem. Jpn., 69, 1282-1298 J. Synth. Org., Chem. Jpn., 69, 1282-1298 J. Synth. Org., Chem. Jpn., 69, 1282-1298 2011 English Disclose to all
Nakamura, M Nakamura, M Nakamura, M Indium-Catalysed Addition of Carbon Units to Acetylenes: Development of a New C–C bond Formation toward Exploitation of Chemical Resources Indium-Catalysed Addition of Carbon Units to Acetylenes: Development of a New C–C bond Formation toward Exploitation of Chemical Resources Indium-Catalysed Addition of Carbon Units to Acetylenes: Development of a New C–C bond Formation toward Exploitation of Chemical Resources Pure. Appl. Chem., 78, 425-434 Pure. Appl. Chem., 78, 425-434 Pure. Appl. Chem., 78, 425-434 2006 English Disclose to all
徳山英利, 中村正治 徳山英利, 中村正治 マイクロ波照射による反応の迅速化 マイクロ波照射による反応の迅速化 有機合成化学協会誌, 63, 5, 523-538 有機合成化学協会誌, 63, 5, 523-538 , 63, 5, 523-538 2005 Japanese Disclose to all
Nakamura, M, Isobe, H, Nakamura E Nakamura, M, Isobe, H, Nakamura E Nakamura, M, Isobe, H, Nakamura E Cyclopropenpne Acetals-synthesis and Reactions Cyclopropenpne Acetals-synthesis and Reactions Cyclopropenpne Acetals-synthesis and Reactions Chem. Rev., 103, 1295-1326 Chem. Rev., 103, 1295-1326 Chem. Rev., 103, 1295-1326 2003 English Disclose to all
Title language:
Conference Activities & Talks
Title Title(Japanese) Title(English) Conference Conference(Japanese) Conference(English) Promotor Promotor(Japanese) Promotor(English) Date Language Assortment Disclose
Exploring Synthetic Opportunities of Iron Catalysis in Sustainable Chemistry[Invited] Exploring Synthetic Opportunities of Iron Catalysis in Sustainable Chemistry [Invited] Exploring Synthetic Opportunities of Iron Catalysis in Sustainable Chemistry [Invited] International Conference on Emerging Trends in Chemistry International Conference on Emerging Trends in Chemistry International Conference on Emerging Trends in Chemistry 2019/07/14 English Oral presentation(invited, special) Disclose to all
Dreaming up World-Changing Catalyst: Utilization of Iron and Wood in Organic Synthesis[Invited] Dreaming up World-Changing Catalyst: Utilization of Iron and Wood in Organic Synthesis [Invited] Dreaming up World-Changing Catalyst: Utilization of Iron and Wood in Organic Synthesis [Invited] Core-to-Core and GTR Symposium on Elements Function for Transformative Catalysis and Materials Core-to-Core and GTR Symposium on Elements Function for Transformative Catalysis and Materials Core-to-Core and GTR Symposium on Elements Function for Transformative Catalysis and Materials 2019/02/07 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Oxidative C–H Amination of Diaryl Amines for the Synthesis of Hole Transfer Materials[Invited] Iron-Catalyzed Oxidative C–H Amination of Diaryl Amines for the Synthesis of Hole Transfer Materials [Invited] Iron-Catalyzed Oxidative C–H Amination of Diaryl Amines for the Synthesis of Hole Transfer Materials [Invited] The International Symposium onThe International Symposium on Catalysis and Fine Chemicals 2018 (C&FC2018)) The International Symposium onThe International Symposium on Catalysis and Fine Chemicals 2018 (C&FC2018)) The International Symposium onThe International Symposium on Catalysis and Fine Chemicals 2018 (C&FC2018)) 2018/12/13 English Oral presentation(invited, special) Disclose to all
化学資源を活用する有機合成化学の開拓―鉄と森で豊かな社会を－[Invited] 化学資源を活用する有機合成化学の開拓―鉄と森で豊かな社会を－ [Invited] 日本化学会第98春季年会 日本化学会第98春季年会 2018/03/21 Japanese Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Oxidative C-H Amination of Diaryl Amines for the Synthesis of Hole Transport Materials[Invited] Iron-Catalyzed Oxidative C-H Amination of Diaryl Amines for the Synthesis of Hole Transport Materials [Invited] Iron-Catalyzed Oxidative C-H Amination of Diaryl Amines for the Synthesis of Hole Transport Materials [Invited] International CLS Forum International CLS Forum International CLS Forum 2018/03/03 English Oral presentation(invited, special) Disclose to all
化学資源を活用する有機合成化学の開拓[Invited] 化学資源を活用する有機合成化学の開拓 [Invited] 有機合成化学協会近畿支部有機合成2月セミナー 有機合成化学協会近畿支部有機合成2月セミナー 2018/02/05 Japanese Oral presentation(invited, special) Disclose to all
ron-Catalyzed Oxidative Amination via Bimetallic Mechanism[Invited] ron-Catalyzed Oxidative Amination via Bimetallic Mechanism [Invited] ron-Catalyzed Oxidative Amination via Bimetallic Mechanism [Invited] Core-to-Core Joint Symposium, Queen's University, Kyoto University, Munster University, Nagoya University Core-to-Core Joint Symposium, Queen's University, Kyoto University, Munster University, Nagoya University Core-to-Core Joint Symposium, Queen's University, Kyoto University, Munster University, Nagoya University 2018/02/02 English Oral presentation(invited, special) Disclose to all
化学資源を活用する有機合成化学の開拓[Invited] 化学資源を活用する有機合成化学の開拓 [Invited] 統合物質創製化学研究推進機構第3回国内シンポジウム 統合物質創製化学研究推進機構第3回国内シンポジウム 2017/10/30 Japanese Oral presentation(invited, special) Disclose to all
化学資源を活用する有機合成化学の開拓[Invited] 化学資源を活用する有機合成化学の開拓 [Invited] H29有機合成化学協会北陸セミナー H29有機合成化学協会北陸セミナー 2017/10/07 Japanese Oral presentation(invited, special) Disclose to all
Stereoselective Trapping of Alkyl Radicals under Iron Catalysis[Invited] Stereoselective Trapping of Alkyl Radicals under Iron Catalysis [Invited] Stereoselective Trapping of Alkyl Radicals under Iron Catalysis [Invited] Nordic/Kyoto OMCOS Nordic/Kyoto OMCOS Nordic/Kyoto OMCOS 2017/06/23 English Oral presentation(invited, special) Disclose to all
Studies on Selective Synthetic Organic Reactions Catalyzed by Iron[Invited] Studies on Selective Synthetic Organic Reactions Catalyzed by Iron [Invited] Studies on Selective Synthetic Organic Reactions Catalyzed by Iron [Invited] 日本化学会第97春季年会 日本化学会第97春季年会 日本化学会第97春季年会 2017/03 Disclose to all
化学資源を活用する精密有機合成反応の開拓[Invited] 化学資源を活用する精密有機合成反応の開拓 [Invited] 平成28年度有機合成化学研究所講演会 平成28年度有機合成化学研究所講演会 2016/11/22 Japanese Oral presentation(invited, special) Disclose to all
Organometallic Carbon–Carbon and Carbon–Heteroatom Bond Forming Reactions Controlled by Iron Catalysts[Invited] Organometallic Carbon–Carbon and Carbon–Heteroatom Bond Forming Reactions Controlled by Iron Catalysts [Invited] Organometallic Carbon–Carbon and Carbon–Heteroatom Bond Forming Reactions Controlled by Iron Catalysts [Invited] 2016 Base Metal Catalysis Symposium 2016 Base Metal Catalysis Symposium 2016 Base Metal Catalysis Symposium 2016/09/02 English Oral presentation(invited, special) Disclose to all
Enantioselective Cross-Coupling and Some Related Reactions under Iron Catalysis[Invited] Enantioselective Cross-Coupling and Some Related Reactions under Iron Catalysis [Invited] Enantioselective Cross-Coupling and Some Related Reactions under Iron Catalysis [Invited] 2016 JST–NTU Joint Seminar on Sustainable Synthesis and Catalysis 2016 JST–NTU Joint Seminar on Sustainable Synthesis and Catalysis 2016 JST–NTU Joint Seminar on Sustainable Synthesis and Catalysis 2016/08/03 English Oral presentation(invited, special) Disclose to all
鉄触媒精密カップリング反応：「使える反応」を目指して[Invited] 鉄触媒精密カップリング反応：「使える反応」を目指して [Invited] 塩野義製薬プロセス研究所講演会 塩野義製薬プロセス研究所講演会 2016/07/12 Japanese Oral presentation(invited, special) Disclose to all
Enantioselective Carbometalation/Ring-Opening Reactions of Oxa- and Azabicyclic Alkenes under Iron Catalysis[Invited] Enantioselective Carbometalation/Ring-Opening Reactions of Oxa- and Azabicyclic Alkenes under Iron Catalysis [Invited] Enantioselective Carbometalation/Ring-Opening Reactions of Oxa- and Azabicyclic Alkenes under Iron Catalysis [Invited] Core-to-Core Joint Symposium Core-to-Core Joint Symposium Core-to-Core Joint Symposium 2016/06/28 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Diborylation, Carboborylation, and Carbosilylation of Alkynes[Invited] Iron-Catalyzed Diborylation, Carboborylation, and Carbosilylation of Alkynes [Invited] Iron-Catalyzed Diborylation, Carboborylation, and Carbosilylation of Alkynes [Invited] BORAM2016 BORAM2016 BORAM2016 2016/06/27 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Selective Cross-Coupling and Some Related Reactions[Invited] Iron-Catalyzed Selective Cross-Coupling and Some Related Reactions [Invited] Iron-Catalyzed Selective Cross-Coupling and Some Related Reactions [Invited] MSD Organic Synthesis Seminar MSD Organic Synthesis Seminar MSD Organic Synthesis Seminar 2016/06/06 English Oral presentation(invited, special) Disclose to all
鉄触媒精密C-CおよびC-Nカップリング反応の開発 ―未活用化学資源の高度利用を目指して―[Invited] 鉄触媒精密C-CおよびC-Nカップリング反応の開発 ―未活用化学資源の高度利用を目指して― [Invited] 横浜国立大学理工学部講演会 横浜国立大学理工学部講演会 2016/02/08 Japanese Oral presentation(invited, special) Disclose to all
Iron-Catalyzed C_H Amination of Aniline Derivatives Iron-Catalyzed C_H Amination of Aniline Derivatives Iron-Catalyzed C_H Amination of Aniline Derivatives Organometallic Chemistry Directed Towards Organic Synthesis: OMCOS18 Organometallic Chemistry Directed Towards Organic Synthesis: OMCOS18 Organometallic Chemistry Directed Towards Organic Synthesis: OMCOS18 2015/06/28 English Oral presentation(invited, special) Disclose to all
ron-Catalyzed C_H Amination of Aniline Derivatives[Invited] ron-Catalyzed C_H Amination of Aniline Derivatives [Invited] ron-Catalyzed C_H Amination of Aniline Derivatives [Invited] The Ninth International Symposium on Integrated Synthesis（ISIS9) The Ninth International Symposium on Integrated Synthesis（ISIS9) The Ninth International Symposium on Integrated Synthesis（ISIS9) 2014/11/14 English Oral presentation(invited, special) Disclose to all
鉄触媒による炭素—炭素および炭素—ヘテロ元素結合生成反応[Invited] 鉄触媒による炭素—炭素および炭素—ヘテロ元素結合生成反応 [Invited] 近畿化学協会ヘテロ原子部会へ伊勢26年度第２回懇話会 近畿化学協会ヘテロ原子部会へ伊勢26年度第２回懇話会 2014/11/08 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒精密カップリング反応[Invited] 鉄触媒精密カップリング反応 [Invited] 中外製薬有機合成化学セミナー 中外製薬有機合成化学セミナー 2014/11/05 Japanese Oral presentation(invited, special) Disclose to all
Controlled Cross-Coupling Reactions with Iron-Bisphosphine Catalysts[Invited] Controlled Cross-Coupling Reactions with Iron-Bisphosphine Catalysts [Invited] Controlled Cross-Coupling Reactions with Iron-Bisphosphine Catalysts [Invited] The 41st International Conference on Coordination Chemistry The 41st International Conference on Coordination Chemistry The 41st International Conference on Coordination Chemistry 2014/07/21 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Aromatic Amination and Related Coupling Reactions[Invited] Iron-Catalyzed Aromatic Amination and Related Coupling Reactions [Invited] Iron-Catalyzed Aromatic Amination and Related Coupling Reactions [Invited] The 17th Joint Symposium of Core-to-Core/IRTG Programs on Elements Function for Transformative Catalysis and Materials The 17th Joint Symposium of Core-to-Core/IRTG Programs on Elements Function for Transformative Catalysis and Materials The 17th Joint Symposium of Core-to-Core/IRTG Programs on Elements Function for Transformative Catalysis and Materials 2014/06/12 English Oral presentation(invited, special) Disclose to all
クロスカップリング反応[Invited] クロスカップリング反応 [Invited] 近畿化学協会有機金属化学セミナー 近畿化学協会有機金属化学セミナー 2014/06/06 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒精密クロスカップリング反応[Invited] 鉄触媒精密クロスカップリング反応 [Invited] 日本化学会九州支部セミナー 日本化学会九州支部セミナー 2014/04/16 Japanese Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Aromatic Amination and Related Coupling Reactions[Invited] Iron-Catalyzed Aromatic Amination and Related Coupling Reactions [Invited] Iron-Catalyzed Aromatic Amination and Related Coupling Reactions [Invited] 7th CaRLa Winter School 2014 7th CaRLa Winter School 2014 7th CaRLa Winter School 2014 2014/02/22 English Oral presentation(invited, special) Disclose to all
Controlled Cross-Coupling Reactions Under Iron-Catalysis: New Mechanism, Reactivity and Selectivity[Invited] Controlled Cross-Coupling Reactions Under Iron-Catalysis: New Mechanism, Reactivity and Selectivity [Invited] Controlled Cross-Coupling Reactions Under Iron-Catalysis: New Mechanism, Reactivity and Selectivity [Invited] 7th CaRLa Winter School 2014 7th CaRLa Winter School 2014 7th CaRLa Winter School 2014 2014/02/22 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Aromatic Amination[Invited] Iron-Catalyzed Aromatic Amination [Invited] Iron-Catalyzed Aromatic Amination [Invited] International Symposium on Catalysis and Fine Chemicals (C&FC) 2013 International Symposium on Catalysis and Fine Chemicals (C&FC) 2013 International Symposium on Catalysis and Fine Chemicals (C&FC) 2013 2013/12/01 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Aromatic Amination and a Few More Relatives[Invited] Iron-Catalyzed Aromatic Amination and a Few More Relatives [Invited] Iron-Catalyzed Aromatic Amination and a Few More Relatives [Invited] The 16th Japan-Korea Seminar on Organic Chemistry The 16th Japan-Korea Seminar on Organic Chemistry The 16th Japan-Korea Seminar on Organic Chemistry 2013/09/27 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Aromatic Amination[Invited] Iron-Catalyzed Aromatic Amination [Invited] Iron-Catalyzed Aromatic Amination [Invited] The 15th Asian Chemical Congress The 15th Asian Chemical Congress The 15th Asian Chemical Congress 2013/08/18 English Oral presentation(invited, special) Disclose to all
Selective Iron-Catalysts for Controlled Organic Synthesis[Invited] Selective Iron-Catalysts for Controlled Organic Synthesis [Invited] Selective Iron-Catalysts for Controlled Organic Synthesis [Invited] The 1st Bristol-Kyoto Symposium The 1st Bristol-Kyoto Symposium The 1st Bristol-Kyoto Symposium 2013/01/10 English Oral presentation(invited, special) Disclose to all
C–C and C–N Cross Coupling Reactions Under High-Oxidation-State Iron Catalys C–C and C–N Cross Coupling Reactions Under High-Oxidation-State Iron Catalys C–C and C–N Cross Coupling Reactions Under High-Oxidation-State Iron Catalys Asian Core Program Lectureship Tour Seminars Asian Core Program Lectureship Tour Seminars Asian Core Program Lectureship Tour Seminars Taipei, ROC Taipei, ROC 2012/11/30 English Oral presentation(invited, special) Disclose to all
Stereoselective C—C Bond Formations under Iron-Catalysis[Invited] Stereoselective C—C Bond Formations under Iron-Catalysis [Invited] Stereoselective C—C Bond Formations under Iron-Catalysis [Invited] Optically Active Compound Symposium Optically Active Compound Symposium Optically Active Compound Symposium Tokyo Tokyo 2012/09/12 English Oral presentation(invited, special) Disclose to all
Selective Cross-Coupling Reactions Catalyzed by Iron-Bisphosphine Complexes[Invited] Selective Cross-Coupling Reactions Catalyzed by Iron-Bisphosphine Complexes [Invited] Selective Cross-Coupling Reactions Catalyzed by Iron-Bisphosphine Complexes [Invited] International Symposium for Advance Chemical Science (ISACS) 7 International Symposium for Advance Chemical Science (ISACS) 7 International Symposium for Advance Chemical Science (ISACS) 7 Edinburgh, UK Edinburgh, UK 2012/06/13 English Oral presentation(invited, special) Disclose to all
Development of Metal-Catalyzed C–C Bond Forming Reactions: An example of interplay of computational modeling and experiment[Invited] Development of Metal-Catalyzed C–C Bond Forming Reactions: An example of interplay of computational modeling and experiment [Invited] Development of Metal-Catalyzed C–C Bond Forming Reactions: An example of interplay of computational modeling and experiment [Invited] JST International Symposium on Multi-scale Simulation of Condensed-phase Reacting Systems (MSCRS2012) JST International Symposium on Multi-scale Simulation of Condensed-phase Reacting Systems (MSCRS2012) JST International Symposium on Multi-scale Simulation of Condensed-phase Reacting Systems (MSCRS2012) Nagoya Nagoya 2012/05/10 English Oral presentation(invited, special) Disclose to all
Development of Metal-Catalyzed C_C Bond Forming Reactions: an example of interplay of computational modeling and experiment[Invited] Development of Metal-Catalyzed C_C Bond Forming Reactions: an example of interplay of computational modeling and experiment [Invited] Development of Metal-Catalyzed C_C Bond Forming Reactions: an example of interplay of computational modeling and experiment [Invited] International Symposium on Multi-scale Simulation of Condensed-phase Reacting Systems (MSCRS2012) International Symposium on Multi-scale Simulation of Condensed-phase Reacting Systems (MSCRS2012) International Symposium on Multi-scale Simulation of Condensed-phase Reacting Systems (MSCRS2012) 2012/03/10 English Oral presentation(invited, special) Disclose to all
Spinning Iron Off in Organic Synthetic Reaction: A New Aspect of Cross-Coupling Reactions[Invited] Spinning Iron Off in Organic Synthetic Reaction: A New Aspect of Cross-Coupling Reactions [Invited] Spinning Iron Off in Organic Synthetic Reaction: A New Aspect of Cross-Coupling Reactions [Invited] The Chinese University of Hong Kong Visiting Scholar Symposium The Chinese University of Hong Kong Visiting Scholar Symposium The Chinese University of Hong Kong Visiting Scholar Symposium Hong Kong Hong Kong 2011/05/05 English Oral presentation(invited, special) Disclose to all
New Development of The Negishi and Suzuki-Miyaura Reactions under Iron Catalysis[Invited] New Development of The Negishi and Suzuki-Miyaura Reactions under Iron Catalysis [Invited] New Development of The Negishi and Suzuki-Miyaura Reactions under Iron Catalysis [Invited] The Chinese University of Hong Kong Organic Chemistry Seminar The Chinese University of Hong Kong Organic Chemistry Seminar The Chinese University of Hong Kong Organic Chemistry Seminar Hong Kong Hong Kong 2011/05/03 English Oral presentation(invited, special) Disclose to all
Iron-catalyzed cross-coupling reaction: an effective method of alkylating various organometallic reagents[Invited] Iron-catalyzed cross-coupling reaction: an effective method of alkylating various organometallic reagents [Invited] Iron-catalyzed cross-coupling reaction: an effective method of alkylating various organometallic reagents [Invited] The International Chemical Congress of Pacific Basin Societies (Pacifichem 2010) The International Chemical Congress of Pacific Basin Societies (Pacifichem 2010) The International Chemical Congress of Pacific Basin Societies (Pacifichem 2010) Honolulu, Hawaii, USA Honolulu, Hawaii, USA 2010/12/17 English Oral presentation(invited, special) Disclose to all
Controlled Cross-Coupling Reactions under Iron-Catalysis: New Mechanism, Reactivity and Selectivity[Invited] Controlled Cross-Coupling Reactions under Iron-Catalysis: New Mechanism, Reactivity and Selectivity [Invited] Controlled Cross-Coupling Reactions under Iron-Catalysis: New Mechanism, Reactivity and Selectivity [Invited] ICR-Chiang Mai University Bilateral Symposium ICR-Chiang Mai University Bilateral Symposium ICR-Chiang Mai University Bilateral Symposium Chiang Mai, Thailand Chiang Mai, Thailand 2010/12/02 English Oral presentation(invited, special) Disclose to all
Stereoselective C–C Bond Formation under Iron-Catalysis[Invited] Stereoselective C–C Bond Formation under Iron-Catalysis [Invited] Stereoselective C–C Bond Formation under Iron-Catalysis [Invited] Japan-Taiwan Joint Symposium on Innovative Synthesis for New Materials Chemistry Japan-Taiwan Joint Symposium on Innovative Synthesis for New Materials Chemistry Japan-Taiwan Joint Symposium on Innovative Synthesis for New Materials Chemistry Uji, Kyoto, Japan Uji, Kyoto, Japan 2010/10/04 English Oral presentation(invited, special) Disclose to all
Enantioselective C–C Bond Formation under Iron-Catalysis[Invited] Enantioselective C–C Bond Formation under Iron-Catalysis [Invited] Enantioselective C–C Bond Formation under Iron-Catalysis [Invited] 6th Asian-European Symposium on Metal Mediated Efficient Reactions 6th Asian-European Symposium on Metal Mediated Efficient Reactions 6th Asian-European Symposium on Metal Mediated Efficient Reactions Singapore Singapore 2010/06/08 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Enantioselective Carbometalation/Ring-Opening Reaction of Oxabicycloalkenes[Invited] Iron-Catalyzed Enantioselective Carbometalation/Ring-Opening Reaction of Oxabicycloalkenes [Invited] Iron-Catalyzed Enantioselective Carbometalation/Ring-Opening Reaction of Oxabicycloalkenes [Invited] BIT’s 1st Annual World Congress of Catalytic Asymmetric Synthesis BIT’s 1st Annual World Congress of Catalytic Asymmetric Synthesis BIT’s 1st Annual World Congress of Catalytic Asymmetric Synthesis Beijing China, Beijing China, 2010/05/21 English Oral presentation(invited, special) Disclose to all
Selective Cross-Coupling Reactions under Iron Catalysis[Invited] Selective Cross-Coupling Reactions under Iron Catalysis [Invited] Selective Cross-Coupling Reactions under Iron Catalysis [Invited] The 3rd International Conference on Joint Project of Chemical Synthesis Core Research Institutions The 3rd International Conference on Joint Project of Chemical Synthesis Core Research Institutions The 3rd International Conference on Joint Project of Chemical Synthesis Core Research Institutions Nagoya Nagoya 2010/01/07 English Oral presentation(invited, special) Disclose to all
鉄触媒による精密炭素ー炭素結合生成反応の開発・空想10年 鉄触媒による精密炭素ー炭素結合生成反応の開発・空想10年 東京工業大学理学研究流動機構シンポジウム「元素化学の可能性」 東京工業大学理学研究流動機構シンポジウム「元素化学の可能性」 東京 東京 2009/12/04 Japanese Oral presentation(invited, special) Disclose to all
鉄族元素を触媒とするクロスカップリング反応の新展開 鉄族元素を触媒とするクロスカップリング反応の新展開 日本農薬学会農薬デザイン研究会 日本農薬学会農薬デザイン研究会 京都 京都 2009/11/27 Japanese Oral presentation(invited, special) Disclose to all
鉄および鉄族元素触媒による高選択的ビアリールカップリング 鉄および鉄族元素触媒による高選択的ビアリールカップリング 社団法人石油学会触媒シンポジウム 社団法人石油学会触媒シンポジウム 東京 東京 2009/11/24 Japanese Oral presentation(invited, special) Disclose to all
クロスカップリング反応における鉄族元素触媒の新展開 クロスカップリング反応における鉄族元素触媒の新展開 第３７回オルガノメタリックセミナー＜最先端分子性機能触媒反応＞ 第３７回オルガノメタリックセミナー＜最先端分子性機能触媒反応＞ 名古屋 名古屋 2009/11/19 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒を用いた精密クロスカップリング反応の最近の進展 鉄触媒を用いた精密クロスカップリング反応の最近の進展 東ソークロスカップリングセミナー 東ソークロスカップリングセミナー 山口 山口 2009/11/02 Japanese Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Suzuki-Miyaura Coupling Reaction Iron-Catalyzed Suzuki-Miyaura Coupling Reaction The 14th Japan-Korea Symposium on Organic Chemistry The 14th Japan-Korea Symposium on Organic Chemistry Shizuoka Shizuoka 2009/10/25 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒による精密クロスカップリング反応 鉄触媒による精密クロスカップリング反応 日本プロセス学会2009サマーシンポジウム 日本プロセス学会2009サマーシンポジウム 東京 東京 2009/07/16 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒による炭素—炭素結合生成反応の精密制御 鉄触媒による炭素—炭素結合生成反応の精密制御 高分子同友会セミナー 高分子同友会セミナー 東京 東京 2009/04/16 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒を活用する精密炭素-炭素結合生成反応 鉄触媒を活用する精密炭素-炭素結合生成反応 日本化学会第89春季年会「第一遷移元素ー触媒作用の新展開」シンポジウム 日本化学会第89春季年会「第一遷移元素ー触媒作用の新展開」シンポジウム 東京 東京 2009/03/28 Japanese Oral presentation(invited, special) Disclose to all
Controlling Iron-Catalysis in Selective Carbon-Carbon Bond Formations[Invited] Controlling Iron-Catalysis in Selective Carbon-Carbon Bond Formations [Invited] Controlling Iron-Catalysis in Selective Carbon-Carbon Bond Formations [Invited] The 3rd International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOA-3) The 3rd International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOA-3) The 3rd International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOA-3) Hangzhou, China Hangzhou, China 2008/09/23 English Oral presentation(invited, special) Disclose to all
Controlling the Iron Catalysis in Cross-Coupling and Some Related Reactions[Invited] Controlling the Iron Catalysis in Cross-Coupling and Some Related Reactions [Invited] Controlling the Iron Catalysis in Cross-Coupling and Some Related Reactions [Invited] The 9th Youngnam-Kinki Joint Symposium on Organometallic Chemistry The 9th Youngnam-Kinki Joint Symposium on Organometallic Chemistry The 9th Youngnam-Kinki Joint Symposium on Organometallic Chemistry Kyoto Kyoto 2008/01/25 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Kumada-Tamao-Corriu and Negishi Coupling Reactions[Invited] Iron-Catalyzed Kumada-Tamao-Corriu and Negishi Coupling Reactions [Invited] Iron-Catalyzed Kumada-Tamao-Corriu and Negishi Coupling Reactions [Invited] International Symposium on Catalyst and Fine Chemicals 2007 (C&FC2011) International Symposium on Catalyst and Fine Chemicals 2007 (C&FC2011) International Symposium on Catalyst and Fine Chemicals 2007 (C&FC2011) Singapore Singapore 2007/12/17 English Oral presentation(invited, special) Disclose to all
Iron-Catalyzed Tamao and Negishi Coupling Reactions[Invited] Iron-Catalyzed Tamao and Negishi Coupling Reactions [Invited] Iron-Catalyzed Tamao and Negishi Coupling Reactions [Invited] The 99th National Meeting of the Korean Chemical Society The 99th National Meeting of the Korean Chemical Society The 99th National Meeting of the Korean Chemical Society Seoul, Korea Seoul, Korea 2007/04/18 English Oral presentation(invited, special) Disclose to all
「レアメタル」を用いないクロスカップリング反応[Invited] 「レアメタル」を用いないクロスカップリング反応 [Invited] 「レアメタル」を用いないクロスカップリング反応 [Invited] 近畿化学協会有機金属部会2006年度第４回例会 近畿化学協会有機金属部会2006年度第４回例会 近畿化学協会有機金属部会 近畿化学協会有機金属部会 2007/02/01 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒を用いる新規炭素—炭素結合生成反応[Invited] 鉄触媒を用いる新規炭素—炭素結合生成反応 [Invited] 鉄触媒を用いる新規炭素—炭素結合生成反応 [Invited] 第21回（財）有機合成化学研究所 講演会 第21回（財）有機合成化学研究所 講演会 （財）有機合成化学研究所 （財）有機合成化学研究所 2006/11/29 Japanese Oral presentation(invited, special) Disclose to all
金属複合系反応剤の設計と反応開発[Invited] 金属複合系反応剤の設計と反応開発 [Invited] 金属複合系反応剤の設計と反応開発 [Invited] 特定領域研究「元素相乗系化合物の化学」第一回公開シンポジウム 特定領域研究「元素相乗系化合物の化学」第一回公開シンポジウム 2006/11/13 Japanese Oral presentation(invited, special) Disclose to all
未来に備える有機合成−新反応で地球の資源を大切に−[Invited] 未来に備える有機合成−新反応で地球の資源を大切に− [Invited] 未来に備える有機合成−新反応で地球の資源を大切に− [Invited] 第13回京都大学化学研究所公開講演 第13回京都大学化学研究所公開講演 京都大学化学研究所 京都大学化学研究所 2006/10/15 Japanese Oral presentation(invited, special) Disclose to all
鉄触媒によるハロアルカン類の交差カップリング反応[Invited] 鉄触媒によるハロアルカン類の交差カップリング反応 [Invited] 鉄触媒によるハロアルカン類の交差カップリング反応 [Invited] 触媒化学討論会 触媒化学討論会 2006/09/26 Japanese Oral presentation(invited, special) Disclose to all
化学資源活用型の新規合成反応の開発[Invited] 化学資源活用型の新規合成反応の開発 [Invited] 化学資源活用型の新規合成反応の開発 [Invited] 日本薬学会東海支部特別講演会・静岡県立大学講演会 日本薬学会東海支部特別講演会・静岡県立大学講演会 2006/09/22 Japanese Oral presentation(invited, special) Disclose to all
レアメタルを使わないクロスカップリング反応：化学資源活用型の有機合成にむけて[Invited] レアメタルを使わないクロスカップリング反応：化学資源活用型の有機合成にむけて [Invited] レアメタルを使わないクロスカップリング反応：化学資源活用型の有機合成にむけて [Invited] 日本薬学会東北支部有機化学若手研究者セミナー 日本薬学会東北支部有機化学若手研究者セミナー 2006/09/16 Japanese Oral presentation(invited, special) Disclose to all
化学資源の活用を目指した新規炭素ー炭素結合生成反応の開発[Invited] 化学資源の活用を目指した新規炭素ー炭素結合生成反応の開発 [Invited] 化学資源の活用を目指した新規炭素ー炭素結合生成反応の開発 [Invited] 有機反応懇談会 有機反応懇談会 2006/08/03 Japanese Oral presentation(invited, special) Disclose to all
塩化アルキル類の鉄触媒による高度分子変換[Invited] 塩化アルキル類の鉄触媒による高度分子変換 [Invited] 塩化アルキル類の鉄触媒による高度分子変換 [Invited] 特定領域研究「炭素資源の高度分子変換」第一回公開シンポジウム 特定領域研究「炭素資源の高度分子変換」第一回公開シンポジウム 2006/06/22 Japanese Oral presentation(invited, special) Disclose to all
炭素と炭素をつなげる新反応：化学資源の活用を念頭に置いた有機合成反応の開発研究[Invited] 炭素と炭素をつなげる新反応：化学資源の活用を念頭に置いた有機合成反応の開発研究 [Invited] 炭素と炭素をつなげる新反応：化学資源の活用を念頭に置いた有機合成反応の開発研究 [Invited] 大阪府立大学白鷺セミナー 大阪府立大学白鷺セミナー 大阪府立大学 大阪府立大学 2006/06/08 Japanese Oral presentation(invited, special) Disclose to all
化学資源の活用を目指した有機合成反応の探求[Invited] 化学資源の活用を目指した有機合成反応の探求 [Invited] 化学資源の活用を目指した有機合成反応の探求 [Invited] 京都大学分子工学コロキウム 京都大学分子工学コロキウム 2006/05/12 Japanese Oral presentation(invited, special) Disclose to all

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Author Author(Japanese) Author(English) Title Title(Japanese) Title(English) Publisher Publisher(Japanese) Publisher(English) Publication date Language Type Disclose
中村正治, 畠山琢次, 今吉隆治, 仲嶋 翔 中村正治, 畠山琢次, 今吉隆治, 仲嶋 翔 金属化合物を触媒とする反応 19･3･7 「鉄」 金属化合物を触媒とする反応 19･3･7 「鉄」 有機合成化学実験法ハンドブック, 丸善 有機合成化学実験法ハンドブック, 丸善 2015 Disclose to all
河村伸太郎, 中川尚久, 中村正治 河村伸太郎, 中川尚久, 中村正治 第11, 12族金属化合物 第11, 12族金属化合物 有機合成化学実験法ハンドブック, 丸善 有機合成化学実験法ハンドブック, 丸善 2014 Disclose to all
中村正治, 仲嶋 翔, 橋本 徹, 畠山琢次 中村正治, 仲嶋 翔, 橋本 徹, 畠山琢次 鉄触媒による不活性ハロゲン化アルキル類の鈴木–宮浦カップリング反応 鉄触媒による不活性ハロゲン化アルキル類の鈴木–宮浦カップリング反応 触媒の設計・反応制御 事例集, pp617–622, 技術情報協会編 触媒の設計・反応制御 事例集, pp617–622, 技術情報協会編 2013 Disclose to all
橋本徹, 清家弘史, 中村正治 橋本徹, 清家弘史, 中村正治 Grignard反応 Grignard反応 トップドラッグから学ぶ創薬化学, 第II部1章, p. 115, 東京化学同人 トップドラッグから学ぶ創薬化学, 第II部1章, p. 115, 東京化学同人 2012 Disclose to all
河村伸太郎, 清家弘史, 中村正治 河村伸太郎, 清家弘史, 中村正治 有機銅反応剤（共役付加） 有機銅反応剤（共役付加） トップドラッグから学ぶ創薬化学, 第II部7章, p. 122, 東京化学同人 トップドラッグから学ぶ創薬化学, 第II部7章, p. 122, 東京化学同人 2012 Disclose to all
中村 正治畠山琢次, 中村正治 中村 正治畠山琢次, 中村正治 均一系鉄触媒による炭素—炭素結合生成反応 均一系鉄触媒による炭素—炭素結合生成反応 CSJカレントヴュー 未来を拓く元素戦略，Part II, 1章, pp. 28–38 CSJカレントヴュー 未来を拓く元素戦略，Part II, 1章, pp. 28–38 2012 Disclose to all
橋本士雄磨, 清家弘史, 中村正治 橋本士雄磨, 清家弘史, 中村正治 Williamsonエーテル合成 Williamsonエーテル合成 トップドラッグから学ぶ創薬化学, 第II部34章, p. 156, 東京化学同人 トップドラッグから学ぶ創薬化学, 第II部34章, p. 156, 東京化学同人 2012 Disclose to all
畠山琢次, 中村正治 畠山琢次, 中村正治 グリニャールクロスカップリング反応 グリニャールクロスカップリング反応 触媒調製ハンドブック, pp. 325–335. 株式会社エヌ・ティー・エス出版 触媒調製ハンドブック, pp. 325–335. 株式会社エヌ・ティー・エス出版 2011 Disclose to all
清家弘史, 中村正治 清家弘史, 中村正治 鉄触媒クロスカップリング反応 鉄触媒クロスカップリング反応 2010 Disclose to all
清家弘史, 中村正治 清家弘史, 中村正治 鉄触媒クロスカップリング反応の進展と展望 鉄触媒クロスカップリング反応の進展と展望 日本初ブロックバスターを目指して -創薬研究の最前線-. pp. 191–209. シーエムシー出版 日本初ブロックバスターを目指して -創薬研究の最前線-. pp. 191–209. シーエムシー出版 2010 Disclose to all
Itoh, S, Nakamura, M Itoh, S, Nakamura, M Itoh, S, Nakamura, M Metal Catalyzed Arylation of Nonactivated Alkyl (Pseudo)Halides via Cross-Coupling Reactions Metal Catalyzed Arylation of Nonactivated Alkyl (Pseudo)Halides via Cross-Coupling Reactions Metal Catalyzed Arylation of Nonactivated Alkyl (Pseudo)Halides via Cross-Coupling Reactions Modern Arylation Methods, Lutz Ackermann, Ed. Chapter 5 Modern Arylation Methods, Lutz Ackermann, Ed. Chapter 5 Modern Arylation Methods, Lutz Ackermann, Ed. Chapter 5 2009 Disclose to all
清家弘史, 中村正治 清家弘史, 中村正治 鉄触媒を用いるクロスカップリング反応の最近の進展 鉄触媒を用いるクロスカップリング反応の最近の進展 触媒年鑑:触媒技術の動向と展望 2009. pp. 28–38. 触媒学会 触媒年鑑:触媒技術の動向と展望 2009. pp. 28–38. 触媒学会 2009 Disclose to all

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Title language:
Industrial Property Rights (Patent)
Inventor(s) Inventor(s) (Japanese) Inventor(s) (English) Title Title(Japanese) Title(English) Stage Patent number Date Disclose
中村 正治, 高谷 光, 畠山 琢次, 鈴木 毅, 今吉 隆治, 青木 雄真, 萩原 秀樹, 曽我 真一 中村 正治, 高谷 光, 畠山 琢次, 鈴木 毅, 今吉 隆治, 青木 雄真, 萩原 秀樹, 曽我 真一 非対称ビス（１，２−ジアリールアミノ）ベンゼン類及びその製造方法 非対称ビス（１，２−ジアリールアミノ）ベンゼン類及びその製造方法 特許公開 特開2017-165722 2017/09/21 Disclose to all
渡辺 隆司, 中村 正治, 高谷 光, 福田 健治, 下平 晴記 渡辺 隆司, 中村 正治, 高谷 光, 福田 健治, 下平 晴記 フェノール誘導体の製造方法 フェノール誘導体の製造方法 特許公開 特開2017-145243 2017/08/24 Disclose to all
渡辺 隆司, 中村 正治, 高谷 光, 勝山 勇, 福田 健治 渡辺 隆司, 中村 正治, 高谷 光, 勝山 勇, 福田 健治 フェノール誘導体の製造方法 フェノール誘導体の製造方法 特許公開 特開2017-145244 2017/08/24 Disclose to all
小野 洋平, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本 士雄磨 小野 洋平, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本 士雄磨 有機電界発光素子用材料、有機電界発光素子、表示装置、及び照明装置 有機電界発光素子用材料、有機電界発光素子、表示装置、及び照明装置 特許公開 特開5819534 2016/08/18 Disclose to all
小野 洋平, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本, 士雄磨小野, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本 士雄磨 小野 洋平, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本, 士雄磨小野, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本 士雄磨 有機電界発光素子用材料、有機電界発光素子、表示装置、及び照明装置 有機電界発光素子用材料、有機電界発光素子、表示装置、及び照明装置 特許公開 特開2015-216380 2015/12/03 Disclose to all
小野 洋平, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本 士雄磨 小野 洋平, 枝連 一志, 生田 利昭, 倪 静萍, 松下 武司, 畠山 琢次, 中村 正治, 橋本 士雄磨 有機電界発光素子用材料、有機電界発光素子、表示装置、及び照明装置 有機電界発光素子用材料、有機電界発光素子、表示装置、及び照明装置 特許公開 特開6298424 2015/10/29 Disclose to all
畠山 琢次, 中村 正治, 橋本 士雄磨 畠山 琢次, 中村 正治, 橋本 士雄磨 多環芳香族化合物 多環芳香族化合物 特許公開 特開5744176 2014/07/17 Disclose to all
畠山琢次, 中村正治, 橋本士雄磨 畠山琢次, 中村正治, 橋本士雄磨 多環芳香族化合物 多環芳香族化合物 特許公開 WO 2012/121398 A1 2013/09/13 Disclose to all
中村 正治, 畠山 琢次, 橋本 徹, 仲嶋 翔, 中川 尚久 中村 正治, 畠山 琢次, 橋本 徹, 仲嶋 翔, 中川 尚久 ビスホスフィン化合物、及びビスホスフィン化合物を配位子とする遷移金属触媒、並びにこれらの製造方法 ビスホスフィン化合物、及びビスホスフィン化合物を配位子とする遷移金属触媒、並びにこれらの製造方法 特許公開 特開5955034 2013/09/12 Disclose to all
中村正治, 畠山琢次, 橋本徹, 仲嶋翔, 中川尚久 中村正治, 畠山琢次, 橋本徹, 仲嶋翔, 中川尚久 ビスホスフィン化合物、及びビスホスフィン化合物を配位子とする遷移金属触媒、並びにこれらの製造方法 ビスホスフィン化合物、及びビスホスフィン化合物を配位子とする遷移金属触媒、並びにこれらの製造方法 特許公開 特開2013-180991 2013/09/12 Disclose to all
畠山 琢次, 橋本 士雄磨, 中村 正治 畠山 琢次, 橋本 士雄磨, 中村 正治 多環芳香族化合物 多環芳香族化合物 特許公開 特開5615261 2012/09/13 Disclose to all
中村 正治, 畠山 琢次, 曽我 真一 中村 正治, 畠山 琢次, 曽我 真一 アリールアミン類の製造方法 アリールアミン類の製造方法 特許公開 特開5777106 2012/06/28 Disclose to all
中村 正治, 畠山 琢次, 藤原 優一 中村 正治, 畠山 琢次, 藤原 優一 クロスカップリング反応用触媒、及びこれを用いた芳香族化合物の製造方法 クロスカップリング反応用触媒、及びこれを用いた芳香族化合物の製造方法 特許公開 特開5622573 2011/12/15 Disclose to all
中村 正治, 畠山 琢次, 吉本 祐也 中村 正治, 畠山 琢次, 吉本 祐也 芳香族アミン化合物の製造方法 芳香族アミン化合物の製造方法 特許公開 特開2010-209017 2010/09/24 Disclose to all
中村正治, 畠山琢次, 吉本祐也 中村正治, 畠山琢次, 吉本祐也 芳香族アミン化合物の製造方法 芳香族アミン化合物の製造方法 特許公開 特開2010-209017 2010/09/24 Disclose to all
畠山琢次, 中村正治, 橋本士雄磨 畠山琢次, 中村正治, 橋本士雄磨 多環芳香族化合物 多環芳香族化合物 特許公開 WO 2010/104047 A1 2010/09/16 Disclose to all
中村 正治, 畠山 琢次 中村 正治, 畠山 琢次 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 特許公開 特開5614985 2010/06/24 Disclose to all
中村正治, 畠山琢次, 藤原優一 中村正治, 畠山琢次, 藤原優一 クロスカップリング反応用触媒，及びこれを用いた芳香族化合物の製造方法 クロスカップリング反応用触媒，及びこれを用いた芳香族化合物の製造方法 特許公開 WO 2010/001640 A1 2010/01/07 Disclose to all
中村 正治, 畠山 琢次, 江口 久雄, 箭野 裕一 中村 正治, 畠山 琢次, 江口 久雄, 箭野 裕一 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 特許公開 特開5156510 2009/12/19 Disclose to all
中村正治, 畠山琢次, 江口久雄, 箭野裕一 中村正治, 畠山琢次, 江口久雄, 箭野裕一 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 特許公開 WO 2009/008447 A1 2009/01/15 Disclose to all
中村正治, 畠山琢次 中村正治, 畠山琢次 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 触媒組成物及びそれを用いたクロスカップリング化合物の製造方法 特許公開 WO 2008/111414 A1 2008/09/18 Disclose to all
中村正治, 伊藤慎庫, 藤田敦子 中村正治, 伊藤慎庫, 藤田敦子 鉄触媒による芳香族化合物の製造方法 鉄触媒による芳香族化合物の製造方法 特許公開 特開2008-214199 2008/09/18 Disclose to all
中村正治, 高瀬俊和, 江口恵二 中村正治, 高瀬俊和, 江口恵二 低温フローNMR測定方法および低温フロー迅速インジェクションNMR 低温フローNMR測定方法および低温フロー迅速インジェクションNMR 特許公開 特開2006-046968 2006/02/16 Disclose to all
中村正治, 中村栄一 中村正治, 中村栄一 カルボニル化合物の製造方法 カルボニル化合物の製造方法 特許公開 特開2005-225846 2005/08/25 Disclose to all
中村正治, 松尾敬子, 伊藤慎庫, 中村栄一 中村正治, 松尾敬子, 伊藤慎庫, 中村栄一 芳香族化合物の製造方法 芳香族化合物の製造方法 特許公開 WO2005/075384 2005/08/18 Disclose to all
中村正治, 遠藤恆平, 中村栄一 中村正治, 遠藤恆平, 中村栄一 βジカルボニル化合物の製法 βジカルボニル化合物の製法 特許公開 特開2005-097193 2005/04/14 Disclose to all

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Title language:
Awards
Title(Japanese) Title(English) Organization name(Japanese) Organization name(English) Date
有機合成化学協会企業冠賞 有機合成化学協会 2020/02/19
第34回学術賞 日本化学会 2017/03/
Banyu young chemist award Banyu Young Chemist Award 2005 萬有生命科学振興財団 2005/11/
Asian Core Program Lectureship Award (Hong Kong) Asian Core Program Lectureship Award (Hong Kong) JSPS Asian CORE Program Project Committee JSPS Asian CORE Program Project Committee 2006/10/
第50回進歩賞 日本化学会 2001/03/
有機合成化学協会研究企画賞 有機合成化学協会（藤沢薬品） 2005/00/00
Asian Core Program Lectureship Award (China) Asian Core Program Lectureship Award (China) JSPS Asian CORE Program Project Committee JSPS Asian CORE Program Project Committee 2006/00/00
Banyu Young Chemist Award 2006 Banyu Young Chemist Award 2006 萬有生命科学振興財団 2006/00/00
External funds: competitive funds and Grants-in-Aid for Scientific Research (Kakenhi)
Type Position Title(Japanese) Title(English) Period
科学技術振興機構さきがけ研究 Representative 不飽和炭化水素を活用する精密合成反応 Development of Carbon—Carbon Bond Formation Reaction Using Feedstock Hydrocarbons -2006/03/31
特定領域研究 Representative 金属複合系反応剤の設計と反応開発 2006-2009
若手研究（Ｓ） Representative 普遍金属を活用する次世代精密有機合成反応の開拓 2008-2012
特別研究員奨励費 Representative 鉄触媒ＣＨ官能基化によるα－アリールカルボン酸類の合成 2012-2014
特別研究員奨励費 Representative 鉄触媒を用いた環境調和型炭素－炭素、炭素－ヘテロ元素結合生成反応の機構研究 2012-2014
挑戦的萌芽研究 Representative 鉄触媒不斉クロスカップリング反応 （平成26年度分） 2014/04/01-2015/03/31
特別研究員奨励費 Representative 鉄触媒ＣＨ官能基化によるα－アリールカルボン酸類の合成 （平成26年度分） 2014/04/01-2015/03/31
挑戦的萌芽研究 Representative 鉄触媒芳香族C-Hアミノ化反応による含窒素多環芳香族化合物の合成 （平成27年度分） 2015/04/01-2016/03/31
特別研究員奨励費 Representative 木質バイオマスの高度利用を志向したリグニン認識型磁性金属ナノ粒子触媒の開発 （平成29年度分） 2017/04/01-2018/03/31
挑戦的研究（萌芽） Representative 森林化学産業創成のための精密木質分子変換反応の開発 （平成30年度分） 2018/04/01-2019/03/31
特別研究員奨励費 Representative 木質バイオマスの高度利用を志向したリグニン認識型磁性金属ナノ粒子触媒の開発 （平成30年度分） 2018/04/01-2019/03/31

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External funds: other than those above
System Main person Title(Japanese) Title(English) Period
最先端・次世代研究開発支援プログラム 中村 正治 レアメタルを凌駕する鉄触媒による精密有機合成化学の開拓 2010-2013
二国間交流事業共同研究・セミナー 中村　正治 低原子価コバルト触媒によるC-H結合活性化反応の反応機構研究 （平成26年度分） 2014/04/01-2015/03/31
二国間交流事業共同研究・セミナー 中村　正治 低原子価コバルト触媒によるC-H結合活性化反応の反応機構研究 （平成27年度分） 2015/04/01-2016/03/31
Teaching subject(s)
Name(Japanese) Name(English) Term Department Period
有機化学I（工業基礎化学）［T15・T18］ 後期 工学部 2011/04-2012/03
有機化学I（工業基礎化学）［T16・T17］ 後期 工学部 2011/04-2012/03
有機金属化学１ 前期 工学研究科 2011/04-2012/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2012/04-2013/03
有機金属化学１ Organotransition Metal Chemistry 1 前期 工学研究科 2012/04-2013/03
物質変換化学 Chemical Transformations 前期 工学研究科 2012/04-2013/03
環境生物・物質化学 Environmental Chemistry and Biochemistry 前期 地球環境学舎 2012/04-2013/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2013/04-2014/03
有機金属化学１ Organotransition Metal Chemistry 1 前期 工学研究科 2013/04-2014/03
環境生物・物質化学 Environmental Chemistry and Biochemistry 前期 地球環境学舎 2013/04-2014/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2014/04-2015/03
有機金属化学１ Organotransition Metal Chemistry 1 前期 工学研究科 2014/04-2015/03
物質変換化学 Chemical Transformations 前期 工学研究科 2014/04-2015/03
環境生物・物質化学 Environmental Chemistry and Biochemistry 前期 地球環境学舎 2014/04-2015/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2015/04-2016/03
物質変換化学 Chemical Transformations 前期 工学研究科 2015/04-2016/03
環境生物・物質化学 Environmental Chemistry and Biochemistry 前期 地球環境学舎 2015/04-2016/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2016/04-2017/03
有機金属化学１ Organotransition Metal Chemistry 1 前期 工学研究科 2016/04-2017/03
物質変換化学 Chemical Transformations 前期 工学研究科 2016/04-2017/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2017/04-2018/03
物質変換化学 Chemical Transformations 前期 工学研究科 2017/04-2018/03
環境生物・物質化学 Environmental Chemistry and Biochemistry 前期 地球環境学舎 2017/04-2018/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2018/04-2019/03
有機金属化学１ Organotransition Metal Chemistry 1 前期 工学研究科 2018/04-2019/03
物質変換化学 Chemical Transformations 前期 工学研究科 2018/04-2019/03
有機化学I（工業基礎化学） Organic Chemistry I (Fundamental Chemistry) 後期 工学部 2019/04-2020/03
物質変換化学 Chemical Transformations 前期 工学研究科 2019/04-2020/03

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School management (title, position)
Title Period
元素科学国際研究センター長 2013/04/01-2015/03/31
国際高等教育院　企画評価専門委員会分野別部会委員（化学部会） 2014/06/01-2015/04/30
国際教育委員会国際学生交流委員会アムジェン・スカラーズ・プログラム小委員会 委員 2016/12/01-2018/03/31
国際高等教育院 企画評価専門委員会 化学部会 委員 2015/05/01-2018/03/31
Faculty management (title, position)
Title Period
全学共通教育システム委員会基礎教育専門委員会化学部会委員 2012/04/01-2014/03/31
化学研究所運営委員会委員 2013/04/01-2014/03/31
化学研究所自己点検評価委員会委員 2013/04/01-2014/03/31
化学研究所設備運営委員会委員 2013/04/01-2014/03/31
化学研究所ゲノムネット推進室運営委員会委員 2014/04/01-2016/03/31
化学研究所運営委員会委員 2014/04/01-2015/03/31
化学研究所自己点検評価委員会委員 2014/04/01-2015/03/31
化学研究所将来問題・研究活性化委員会委員 2014/04/01-2015/03/31
化学研究所広報委員会委員 2015/04/01-2016/03/31
化学研究所産学連携委員会委員 2015/04/01-2016/03/31
化学研究所将来問題・研究活性化委員会委員 2015/04/01-2016/03/31
宇治キャンパス危機管理委員会 2016/04/01-0000
宇治地区総合環境安全管理センター運営委員会 2016/04/01-2018/03/31
化学研究所将来問題・研究活性化委員会委員 2016/04/01-2017/03/31
化学研究所産学連携委員会委員 2016/04/01-2017/03/31
京都大学宇治キャンパス公開2020実行委員会 2017/01/01-2017/12/31
化学研究所安全衛生委員会委員長 2017/04/01-2018/03/31
化学研究所情報セキュリティ委員会委員 2017/04/01-2018/03/31
化学研究所安全衛生委員会委員長 2018/04/01-2019/03/31
化学研究所情報セキュリティ委員会委員 2018/04/01-2019/03/31
化学研究所産学連携委員会委員 2018/04/01-2019/03/31
宇治地区総合環境安全管理センター運営委員会 2018/04/01-2020/03/31
化学研究所安全衛生委員会委員長 2019/04/01-2020/03/31
化学研究所情報セキュリティ委員会委員 2019/04/01-2020/03/31
化学研究所産学連携委員会委員 2019/04/01-2020/03/31

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