Stereoselective synthesis of C3-tetrasubstituted oxindoles <i>via</i> copper catalyzed asymmetric propargylation-Reference-Cited by-同舟云学术

Stereoselective synthesis of C3-tetrasubstituted oxindoles via copper catalyzed asymmetric propargylation

Published:2022 Issue:41 Volume:12 Page:26727-26732
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Wang Jiao-Mei¹,Zhao Yu²,Yao Chang-Sheng³^ORCID,Zhang Kai³^ORCID

Affiliation:

1. School of Materials and Chemical Engineering, Xuzhou University of Technology, Xuzhou 221018, P. R. China

2. College of Chemistry and Chemical Engineering, Yan'an University, Yan'an, Shaanxi 716000, P. R. China

3. Jiangsu Key Lab of Green Synthetic Chemistry for Functional Materials, School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou, Jiangsu 221116, P. R. China

Abstract

Herein, a copper catalyzed asymmetric propargylation of 2-oxindole-3-carboxylate esters with terminal propargylic esters is described.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Xuzhou Institute of Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA04603B

Reference108 articles.

1. Catalytic Asymmetric Synthesis of Either Enantiomer of the Calabar Alkaloids Physostigmine and Physovenine

2. Total Synthesis of Spirotryprostatin A, Leading to the Discovery of Some Biologically Promising Analogues

3. Total Synthesis of (−)-Spirotryprostatin B and Three Stereoisomers

4. The Asymmetric Total Synthesis of (+)- and (−)-Spirotryprostatin B

5. First Total Synthesis of (±)-Strychnofoline via a Highly Selective Ring-Expansion Reaction

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