Palladium‐Catalyzed Highly Enantioselective Arylation of Cyclic N ‐Sulfonyl α‐Ketimino Esters towards the Synthesis of α‐Quaternary Chiral Amino Acid Derivatives-Reference-Cited by-同舟云学术

Palladium‐Catalyzed Highly Enantioselective Arylation of Cyclic N ‐Sulfonyl α‐Ketimino Esters towards the Synthesis of α‐Quaternary Chiral Amino Acid Derivatives

Published:2019-12-23 Issue:4 Volume:12 Page:1129-1133
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Wu Chun‐Yan¹,Xu Ming‐Hua¹²^ORCID

Affiliation:

1. State Key Laboratory of Drug Research Shanghai Institute of Materia MedicaChinese Academy of Sciences 555 Zuchongzhi Road Shanghai 201203 P. R. China

2. Shenzhen Grubbs Institute and Department of ChemistrySouthern University of Science and Technology 1088 Xueyuan Boulevard Shenzhen 518055 P. R. China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.201901933

Reference79 articles.

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4. Metabotropic Glutamate Receptor Subtypes as Targets for Neuroprotective Drugs

5. Asymmetric synthesis of (S)-1-aminoindan-1,5-dicarboxylic acid and related analogues via intramolecular acylation of enantiopure α,α-disubstituted amino acids

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