A facile synthesis of isoindoline and Δ1-pyrrolines from chalcone and glycine by a cascade of process involving addition, in situ decarboxylation, and cyclization-Reference-Cited by-同舟云学术

A facile synthesis of isoindoline and Δ1-pyrrolines from chalcone and glycine by a cascade of process involving addition, in situ decarboxylation, and cyclization

Published:2014-07 Issue:29 Volume:55 Page:3992-3995
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Elamparuthi Elangovan,Sarathkumar Subramaniayan,Girija Swaminathan,Anbazhagan Veerappan

Funder

Department of Science, Government of India

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference41 articles.

1. Synthesis and activity of spiroisoindolines as novel noncompetitive NMDA antagonists

2. 1,3-Diaryl-4,5,6,7-tetrahydro-2H-isoindole Derivatives: A New Series of Potent and Selective COX-2 Inhibitors in Which a Sulfonyl Group Is Not a Structural Requisite

3. Isoindolines: A new series of potent and selective endothelin-A receptor antagonists

4. Isoindolo[2,1-c]benzo[1,2,4]triazines: A new ring system with antiproliferative activity

5. Isoindolo[2,1-a]quinoxaline Derivatives, Novel Potent Antitumor Agents with Dual Inhibition of Tubulin Polymerization and Topoisomerase I

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