Development of Pseudo-C2-symmetric Chiral Binaphthyl Monocarboxylic Acids for Enantioselective C(sp3)–H Functionalization Reactions under Rh(III) Catalysis-Reference-Cited by-同舟云学术

Development of Pseudo-C2-symmetric Chiral Binaphthyl Monocarboxylic Acids for Enantioselective C(sp3)–H Functionalization Reactions under Rh(III) Catalysis

Published:2021-03-22 Issue:7 Volume:11 Page:4271-4277
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Kato Yoshimi¹,Lin Luqing²^ORCID,Kojima Masahiro¹^ORCID,Yoshino Tatsuhiko¹^ORCID,Matsunaga Shigeki¹³^ORCID

Affiliation:

1. Faculty of Pharmaceutical Science, Hokkaido University, Sapporo 060-0812, Japan

2. Zhang Dayu School of Chemistry, Dalian University of Technology, Dalian 116024, Liaoning, China

3. Global Station for Biosurfaces and Drug Discovery, Hokkaido University, Sapporo 060-0812, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.1c00765

Reference79 articles.

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2. Mild metal-catalyzed C–H activation: examples and concepts

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4. Transition-Metal-Catalyzed C–H Bond Addition to Carbonyls, Imines, and Related Polarized π Bonds

5. Transition-Metal-Catalyzed Selective Functionalization of C(sp3 )−H Bonds in Natural Products

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