Base-induced conversion of 5-aminothiazolium salts into substituted pyrroles and pyrrolines via 1,3-dipolar cycloadditions with electron-deficient alkynes and alkenes-Reference-Cited by-同舟云学术

Base-induced conversion of 5-aminothiazolium salts into substituted pyrroles and pyrrolines via 1,3-dipolar cycloadditions with electron-deficient alkynes and alkenes

Published:1995-06 Issue:25 Volume:51 Page:7019-7034
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Berrée Fabienne,Morel Georges

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. The Preparation and Properties of Mesoionic 5-Iminothiazole Derivatives

2. Mesoionic 5-Acylimino-2-methylthiothiazoles

3. Three-component cyclocondensations. Two methods for the efficient preparation of 5-aminothiazolium salts via the reaction of isocyanides either with dimethylthioformamide and imino chloro sulfides or benzaldimines and aryl chlorothioformates

4. Meso-ionic heterocycles (1976–1980)

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