Ni-Catalyzed Enantioselective C-Acylation of α-Substituted Lactams-Reference-Cited by-同舟云学术

Ni-Catalyzed Enantioselective C-Acylation of α-Substituted Lactams

Published:2016-07-15 Issue:29 Volume:138 Page:8997-9000
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hayashi Masaki¹,Bachman Shoshana¹,Hashimoto Satoshi¹,Eichman Chad C.¹²,Stoltz Brian M.¹

Affiliation:

1. The Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States

2. Department of Chemistry and Biochemistry, Loyola University, Chicago, Illinois 60660, United States

Funder

Daiichi-Sankyo

Ministry of Education, Culture, Sports, Science, and Technology

Japan Society for the Promotion of Science

Loyola University Chicago

National Institute of General Medical Sciences

California Institute of Technology

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.6b02120

Reference48 articles.

1. Asymmetric Catalysis Special Feature Part I: Catalytic asymmetric synthesis of all-carbon quaternary stereocenters

2. Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters

3. Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems

4. Catalytic enantioselective synthesis of quaternary carbon stereocentres

5. Catalytic Enantioselective Construction of Quaternary Stereocenters: Assembly of Key Building Blocks for the Synthesis of Biologically Active Molecules

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