Binaphthyl-Proline Hybrid Chiral Ligands: Modular Design, Synthesis, and Enantioswitching in Cu(II)-Catalyzed Enantioselective Henry Reactions-Reference-Cited by-同舟云学术

Binaphthyl-Proline Hybrid Chiral Ligands: Modular Design, Synthesis, and Enantioswitching in Cu(II)-Catalyzed Enantioselective Henry Reactions

Published:2022-09-15 Issue: Volume: Page:
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yao Chao¹,Chen Yaoqi¹,Wang Chao¹,Sun Ruize¹,Chang Haotian¹,Jiang Ruiheng¹,Li Lin¹,Wang Xin¹^ORCID,Li Yue-Ming¹^ORCID

Affiliation:

1. State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin300071, China

Funder

National Cancer Center

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c01127

Reference64 articles.

1. Privileged Chiral Catalysts

3. Modified BINOL Ligands in Asymmetric Catalysis

4. BINOL: A Versatile Chiral Reagent

5. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications

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