Nickel-Catalyzed Enantioselective Reductive Conjugate Arylation and Heteroarylation via an Elementary Mechanism of 1,4-Addition-Reference-Cited by-同舟云学术

Nickel-Catalyzed Enantioselective Reductive Conjugate Arylation and Heteroarylation via an Elementary Mechanism of 1,4-Addition

Published:2022-10-31 Issue:44 Volume:144 Page:20249-20257
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhang Luoqiang¹²,Zhao Mengxin¹,Pu Maoping³^ORCID,Ma Zhaoming¹,Zhou Jingsong²,Chen Caiyou⁴^ORCID,Wu Yun-Dong³⁵^ORCID,Chi Yonggui Robin²^ORCID,Zhou Jianrong Steve¹^ORCID

Affiliation:

1. State Key Laboratory of Chemical Oncogenomics, Guangdong Provincial Key Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Room F312, 2199 Lishui Road, Nanshan District, Shenzhen 518055, China

2. School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, 21 Nanyang Link, 637371, Singapore

3. Shenzhen Bay Laboratory, Gaoke Innovation Center, Guangqiao Road, Guangming District, Shenzhen 518107, China

4. College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China

5. Laboratory of Computational Chemistry and Drug Design, State Key Laboratory of Chemical Oncogenomics, Peking University Shenzhen Graduate School, Shenzhen Bay Laboratory, Shenzhen 518055, China

Funder

Shenzhen Bay Laboratory

National Research Foundation Singapore

National Natural Science Foundation of China

Guangdong Provincial Key Laboratory of Chemical Genomics

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Shanghai Jiao Tong University

State Key Laboratory of Chemical Oncogenomics

Peking University Shenzhen Graduate School

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis