Efficient asymmetric Michael reaction of 2-oxindole-3-carboxylate esters with maleimides catalyzed by cinchonidine-Reference-Cited by-同舟云学术

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Efficient asymmetric Michael reaction of 2-oxindole-3-carboxylate esters with maleimides catalyzed by cinchonidine

Published:2014-05 Issue:21 Volume:70 Page:3478-3484
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Zhou Jing,Jia Li-Na,Peng Lin,Wang Qi-Lin,Tian Fang,Xu Xiao-Ying,Wang Li-Xin

Funder

National Natural Science Foundation of China

Western Light Talent Culture Project

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference53 articles.

1. For selected reviews:

2. Gelsemine: A Thought-Provoking Target for Total Synthesis

3. The Asymmetric Intramolecular Heck Reaction in Natural Product Total Synthesis

4. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

5. Selected examples:

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3. Asymmetric Catalysis of Chiral Bifunctional Selenides and Selenonium Salts Bearing a Urea Group;Asian Journal of Organic Chemistry;2021-02-18

4. Organocatalytic asymmetric cascade 1,6-addition/hemiketalization/retro-Henry reaction of ortho-hydroxyphenyl-substituted p-QMs with α-nitroketones;Organic & Biomolecular Chemistry;2020

5. High diastereoselective synthesis of spiro-barbituratechromans via domino oxa-Michael/1,6-addition reactions of ortho-hydroxyphenylsubstituted para-quinone methides with barbiturate-based olefins;Tetrahedron;2019-12

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