Asymmetric Synthesis of Oxindole-Derived Vicinal Tetrasubstituted Acyclic Amino Acid Derivatives by the Mannich-Type Reaction-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Oxindole-Derived Vicinal Tetrasubstituted Acyclic Amino Acid Derivatives by the Mannich-Type Reaction

Published:2020-06-30 Issue:15 Volume:85 Page:9661-9671
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hou Ke-Qiang¹^ORCID,Zhou Feng¹,Chen Xue-Ping¹,Ge Yang¹,Chan Albert S. C.¹^ORCID,Xiong Xiao-Feng¹^ORCID

Affiliation:

1. Guangdong Provincial Key Laboratory of Chiral Molecules and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China

Funder

Government of Guangdong Province

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, Sun Yat-sen University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c00981

Reference49 articles.

1. Enantio‐ and Diastereoselective Construction of α,α‐Disubstituted α‐Amino Acids for the Synthesis of Biologically Active Compounds

2. Recent approaches towards the asymmetric synthesis of α,α-disubstituted α-amino acids

3. Recent Advances in the Asymmetric Synthesis of α-(Trifluoromethyl)-Containing α-Amino Acids

4. Inhibition of Proteasome Activities and Subunit-Specific Amino-Terminal Threonine Modification by Lactacystin

5. Peptidomimetics – A Versatile Route to Biologically Active Compounds

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