中村正治

Last Update: 2019/10/07 14:19:28

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
English

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	Disclose
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
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
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
Isozaki, K.; Shimoaka, T.; Oshiro, S.; Yamaguchi, A.; Pincella, F.; Ueno, R.; Hasegawa, T.; Watanabe, T.; Takaya, H.; Nakamura, M.	Isozaki, K.; Shimoaka, T.; Oshiro, S.; Yamaguchi, A.; Pincella, F.; Ueno, R.; Hasegawa, T.; Watanabe, T.; Takaya, H.; Nakamura, M.	Isozaki, K.; Shimoaka, T.; Oshiro, S.; Yamaguchi, A.; Pincella, F.; Ueno, R.; Hasegawa, T.; Watanabe, T.; Takaya, H.; Nakamura, M.	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, 7483-7493	ACS Omega, 3, 7483-7493	ACS Omega, 3, 7483-7493	2018/07	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
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
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
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
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
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
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
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
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
H. Takaya; S. Nakajima; N. Nakagawa; K. Isozaki; T. Iwamoto; R. Imayoshi; N. Gower; L. Adak; T. Hatakeyama; T. Honma; M. Takagi; Y. Sunada; H. Nagashima; D. Hashizume; O. Takahashi; M. Nakamura	H. Takaya; S. Nakajima; N. Nakagawa; K. Isozaki; T. Iwamoto; R. Imayoshi; N. Gower; L. Adak; T. Hatakeyama; T. Honma; M. Takagi; Y. Sunada; H. Nagashima; D. Hashizume; O. Takahashi; M. Nakamura	H. Takaya; S. Nakajima; N. Nakagawa; K. Isozaki; T. Iwamoto; R. Imayoshi; N. Gower; L. Adak; T. Hatakeyama; T. Honma; M. Takagi; Y. Sunada; H. Nagashima; D. Hashizume; O. Takahashi; M. Nakamura	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	2015/01	Refereed	English	Disclose to all
N. Nakagawa; T. Hatakeyama; M. Nakamura	N. Nakagawa; T. Hatakeyama; M. Nakamura	N. Nakagawa; T. Hatakeyama; M. Nakamura	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	2015/01	Refereed	English	Disclose to all
N. Nakagawa; T. Hatakeyama; M. Nakamura	N. Nakagawa; T. Hatakeyama; M. Nakamura	N. Nakagawa; T. Hatakeyama; M. Nakamura	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	2014/12	Refereed	English	Disclose to all
S. Hashimoto; T. Ikuta; K. Shiren; S. Nakatsuka; J. Ni, M. Nakamura, T. Hatakeyama	S. Hashimoto; T. Ikuta; K. Shiren; S. Nakatsuka; J. Ni, M. Nakamura, T. Hatakeyama	S. Hashimoto; T. Ikuta; K. Shiren; S. Nakatsuka; J. Ni, M. Nakamura, T. Hatakeyama	Triplet-Energy Control of Polycyclic Aromatic Hydrocarbons by BN Replacement: Development of Ambipolar Host Materials for Phosphorescent OLEDs	Triplet-Energy Control of Polycyclic Aromatic Hydrocarbons by BN Replacement: Development of Ambipolar Host Materials for Phosphorescent OLEDs	Triplet-Energy Control of Polycyclic Aromatic Hydrocarbons by BN Replacement: Development of Ambipolar Host Materials for Phosphorescent OLEDs	Chemistry of Materials, 26, 21, 6265-6271	Chemistry of Materials, 26, 21, 6265-6271	Chemistry of Materials, 26, 21, 6265-6271	2014/10	Refereed	English	Disclose to all
Y. Aoki; R. Imayoshi; T. Hatakeyama; H. Takaya; M. Nakamura	Y. Aoki; R. Imayoshi; T. Hatakeyama; H. Takaya; M. Nakamura	Y. Aoki; R. Imayoshi; T. Hatakeyama; H. Takaya; M. Nakamura	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 (Kuwajima Special Issue), 90, 2, 893-900	Heterocycles (Kuwajima Special Issue), 90, 2, 893-900	Heterocycles (Kuwajima Special Issue), 90, 2, 893-900	2014/10	Refereed	English	Disclose to all
S. Hashimoto, S. Nakatsuka, M. Nakamura, T. Hatakeyama	S. Hashimoto, S. Nakatsuka, M. Nakamura, T. Hatakeyama	S. Hashimoto, S. Nakatsuka, M. Nakamura, T. Hatakeyama	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	2014/10	Refereed	English	Disclose to all
R. Agata; T. Iwamoto; N. Nakagawa; K. Isozak; T. Hatakeyama; H. Takaya; M. Nakamura	R. Agata; T. Iwamoto; N. Nakagawa; K. Isozak; T. Hatakeyama; H. Takaya; M. Nakamura	R. Agata; T. Iwamoto; N. Nakagawa; K. Isozak; T. Hatakeyama; H. Takaya; M. Nakamura	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, 47, 12, 1733-1740	Synthesis, 47, 12, 1733-1740	Synthesis, 47, 12, 1733-1740	2014	Refereed	English	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
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
R.K. Gabr; T. Hatakeyama; K. Takenaka; S. Takizawa; Y. Okada; M. Nakamura; H. Sasai	R.K. Gabr; T. Hatakeyama; K. Takenaka; S. Takizawa; Y. Okada; M. Nakamura; H. Sasai	R.K. Gabr; T. Hatakeyama; K. Takenaka; S. Takizawa; Y. Okada; M. Nakamura; H. Sasai	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	Disclose to all
T. Hatakeyama; R. Imayoshi; Y. Yoshimoto; S.K. Ghorai; M. Jin; H. Takaya; K. Norisuye; Y. Sohrin; M. Nakamura	T. Hatakeyama; R. Imayoshi; Y. Yoshimoto; S.K. Ghorai; M. Jin; H. Takaya; K. Norisuye; Y. Sohrin; M. Nakamura	T. Hatakeyama; R. Imayoshi; Y. Yoshimoto; S.K. Ghorai; M. Jin; H. Takaya; K. Norisuye; Y. Sohrin; M. Nakamura	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	2012/12	Refereed	English	Disclose to all
T. Hatakeyama; S. Hashimoto; T. Oba; M. Nakamura	T. Hatakeyama; S. Hashimoto; T. Oba; M. Nakamura	T. Hatakeyama; S. Hashimoto; T. Oba; M. Nakamura	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	2012/12	Refereed	English	Disclose to all
K. Fukami; R. Koda; T. Sakka; T. Urata; K.-I. Amano; H. Takaya; M. Nakamura; Y. Ogata; M. Kinoshita	K. Fukami; R. Koda; T. Sakka; T. Urata; K.-I. Amano; H. Takaya; M. Nakamura; Y. Ogata; M. Kinoshita	K. Fukami; R. Koda; T. Sakka; T. Urata; K.-I. Amano; H. Takaya; M. Nakamura; Y. Ogata; M. 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	Refereed	English	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
S.K. Ghorai; M. Jin; T. Hatakeyama; M. Nakamura	S.K. Ghorai; M. Jin; T. Hatakeyama; M. Nakamura	S.K. Ghorai; M. Jin; T. Hatakeyama; M. Nakamura	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	2012/02	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
T. Hashimoto; T. Hatakeyama; M. Nakamura	T. Hashimoto; T. Hatakeyama; M. Nakamura	T. Hashimoto; T. Hatakeyama; M. Nakamura	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	2012/01	Refereed	English	Disclose to all
D. Noda; Y. Sunada; T. Hatakeyama; M. Nakamura; H. Nagashima	D. Noda; Y. Sunada; T. Hatakeyama; M. Nakamura; H. Nagashima	D. Noda; Y. Sunada; T. Hatakeyama; M. Nakamura; H. Nagashima	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	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
T. Hatakeyama; T. Hashimoto; K.K.A.D.S. Kathriarachchi; T. Zenmyo; H. Seike; M. Nakamura	T. Hatakeyama; T. Hashimoto; K.K.A.D.S. Kathriarachchi; T. Zenmyo; H. Seike; M. Nakamura	T. Hatakeyama; T. Hashimoto; K.K.A.D.S. Kathriarachchi; T. Zenmyo; H. Seike; M. Nakamura	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	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
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
T. Hatakeyama; S. Hashimoto; S. Seki; M. Nakamura	T. Hatakeyama; S. Hashimoto; S. Seki; M. Nakamura	T. Hatakeyama; S. Hashimoto; S. Seki; M. Nakamura	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	2011/11	Refereed	English	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
T. Hatakeyama; Y.-I. Fujiwara; Y. Okada; T. Itoh; T. Hashimoto; S. Kawamura; K. Ogata; H. Takaya; M. Nakamura	T. Hatakeyama; Y.-I. Fujiwara; Y. Okada; T. Itoh; T. Hashimoto; S. Kawamura; K. Ogata; H. Takaya; M. Nakamura	T. Hatakeyama; Y.-I. Fujiwara; Y. Okada; T. Itoh; T. Hashimoto; S. Kawamura; K. Ogata; H. Takaya; M. Nakamura	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	2011/09	Refereed	English	Disclose to all
T. Hatakeyama; S. Hashimoto; M. Nakamura	T. Hatakeyama; S. Hashimoto; M. Nakamura	T. Hatakeyama; S. Hashimoto; M. Nakamura	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	2011/04	Refereed	English	Disclose to all
T. Hatakeyama; Y. Okada; Y. Yoshimoto; M. Nakamura	T. Hatakeyama; Y. Okada; Y. Yoshimoto; M. Nakamura	T. Hatakeyama; Y. Okada; Y. Yoshimoto; M. Nakamura	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	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
K. Ishizuka; H. Seike; T. Hatakeyama; M. Nakamura	K. Ishizuka; H. Seike; T. Hatakeyama; M. Nakamura	K. Ishizuka; H. Seike; T. Hatakeyama; M. Nakamura	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	2010/09	Refereed	English	Disclose to all
T. Hatakeyama; T. Hashimoto; Y. Kondo; Y. Fujiwara; H. Seike; H. Takaya; Y. Tamada; T. Ono; M. Nakamura	T. Hatakeyama; T. Hashimoto; Y. Kondo; Y. Fujiwara; H. Seike; H. Takaya; Y. Tamada; T. Ono; M. Nakamura	T. Hatakeyama; T. Hashimoto; Y. Kondo; Y. Fujiwara; H. Seike; H. Takaya; Y. Tamada; T. Ono; M. Nakamura	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	2010/08	Refereed	English	Disclose to all
T. Hatakeyama; Y. Yoshimoto; S.K. Ghorai; M. Nakamura	T. Hatakeyama; Y. Yoshimoto; S.K. Ghorai; M. Nakamura	T. Hatakeyama; Y. Yoshimoto; S.K. Ghorai; M. Nakamura	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	2010/04	Refereed	English	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
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
T. Hatakeyama; N. Nakagawa; M. Nakamura	T. Hatakeyama; N. Nakagawa; M. Nakamura	T. Hatakeyama; N. Nakagawa; M. Nakamura	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	2009/10	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
T. Hatakeyama; S. Hashimoto; K. Ishizuka; M. Nakamura	T. Hatakeyama; S. Hashimoto; K. Ishizuka; M. Nakamura	T. Hatakeyama; S. Hashimoto; K. Ishizuka; M. Nakamura	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	2009/08	Refereed	English	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
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
T. Hatakeyama; Y. Kondo; Y.-I. Fujiwara; H. Takaya; S. Ito; E. Nakamura; M. Nakamura	T. Hatakeyama; Y. Kondo; Y.-I. Fujiwara; H. Takaya; S. Ito; E. Nakamura; M. Nakamura	T. Hatakeyama; Y. Kondo; Y.-I. Fujiwara; H. Takaya; S. Ito; E. Nakamura; M. Nakamura	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	Disclose to all
D. Noda; Y. Sunada; T. Hatakeyama; M. Nakamura; H. Nagashima	D. Noda; Y. Sunada; T. Hatakeyama; M. Nakamura; H. Nagashima	D. Noda; Y. Sunada; T. Hatakeyama; M. Nakamura; H. Nagashima	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	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
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
T. Hatakeyama; Y. Yoshimoto; T. Gabriel; M. Nakamura	T. Hatakeyama; Y. Yoshimoto; T. Gabriel; M. Nakamura	T. Hatakeyama; Y. Yoshimoto; T. Gabriel; M. Nakamura	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	2008/12	Refereed	English	Disclose to all
T. Hatakeyama; M. Nakamura; E. Nakamura	T. Hatakeyama; M. Nakamura; E. Nakamura	T. Hatakeyama; M. Nakamura; E. Nakamura	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	2008/11	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
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
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
T. Hatakeyama; S. Ito; H. Yamane; M. Nakamura; E. Nakamura	T. Hatakeyama; S. Ito; H. Yamane; M. Nakamura; E. Nakamura	T. Hatakeyama; S. Ito; H. Yamane; M. Nakamura; E. Nakamura	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	2007/08	Refereed	English	Disclose to all
T. Hatakeyama; M. Nakamura	T. Hatakeyama; M. Nakamura	T. Hatakeyama; M. Nakamura	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	2007/08	Refereed	English	Disclose to all
K. Endo; T. Hatakeyama; M. Nakamura; E. Nakamura	K. Endo; T. Hatakeyama; M. Nakamura; E. Nakamura	K. Endo; T. Hatakeyama; M. Nakamura; E. Nakamura	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	2007/04	Refereed	English	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
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; 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
T. Hatakeyama; S. Ito; M. Nakamura; E. Nakamura	T. Hatakeyama; S. Ito; M. Nakamura; E. Nakamura	T. Hatakeyama; S. Ito; M. Nakamura; E. Nakamura	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	2005/10	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
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; 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	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; T. Hatakeyama; K. Hara; H. Fukudome; E. Nakamura	M. Nakamura; T. Hatakeyama; K. Hara; H. Fukudome; E. Nakamura	M. Nakamura; T. Hatakeyama; K. Hara; H. Fukudome; E. Nakamura	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	2004/11	Refereed	English	Disclose to all
M. Nakamura; T. Hatakeyama; E. Nakamura	M. Nakamura; T. Hatakeyama; E. Nakamura	M. Nakamura; T. Hatakeyama; E. Nakamura	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	2004/09	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
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; T. Hatakeyama; K. Hara; E. Nakamura	M. Nakamura; T. Hatakeyama; K. Hara; E. Nakamura	M. Nakamura; T. Hatakeyama; K. Hara; E. Nakamura	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	2003/05	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.; 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; 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
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
M. Nakamura; K. Hara; T. Hatakeyama; E. Nakamura	M. Nakamura; K. Hara; T. Hatakeyama; E. Nakamura	M. Nakamura; K. Hara; T. Hatakeyama; E. Nakamura	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	2001/10	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
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; 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
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; 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
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
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
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
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
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
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
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
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; 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
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
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
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
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
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
<< < > >> Title language:

Misc

Author	Author(Japanese)	Author(English)	Title	Title(Japanese)	Title(English)	Bibliography	Bibliography(Japanese)	Bibliography(English)	Publication date	Language	Disclose
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
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
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	Org. React., 83, 1-209	, 83, 1-209	Org. React., 83, 1-209	2014	English	Disclose to all
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	Pure. Appl. Chem., 78, 425-434	, 78, 425-434	Pure. Appl. Chem., 78, 425-434	2006	English	Disclose to all
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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
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
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
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
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
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
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
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
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
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
「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
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				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]	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
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				2018/03/03	English	Oral presentation(invited, special)	Disclose to all
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				2018/02/02	English	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]	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]	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
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				2016/09/02	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]	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
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				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]	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]	MSD Organic Synthesis Seminar		MSD Organic Synthesis Seminar				2016/06/06	English	Oral presentation(invited, special)	Disclose to all
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				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]	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
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				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]	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
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				2014/02/22	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]	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]	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]	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]	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]	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	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]	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]	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]	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]	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]	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]	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]	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]	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]	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]	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]	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]	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
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)	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]	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]	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]	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
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Books etc

Author	Author(Japanese)	Author(English)	Title	Title(Japanese)	Title(English)	Publisher	Publisher(Japanese)	Publisher(English)	Publication date	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
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
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
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
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
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
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	Modern Arylation Methods, Lutz Ackermann, Ed. Chapter 5		Modern Arylation Methods, Lutz Ackermann, Ed. Chapter 5	2009	Disclose to all
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Patents

Inventor(s)	Inventor(s) (Japanese)	Title	Title(Japanese)	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;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
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
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	WO 2012/121398 A1	2013/09/13	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
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
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
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
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，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，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
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;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;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	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;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，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
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
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Awards

Title(Japanese)	Title(English)	Organization name(Japanese)	Organization name(English)	Date
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)	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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中村 正治

中村正治