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Thiazole formation through a modified Gewald reaction.

Published version
Peer-reviewed

Type

Article

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Authors

Mallia, Carl J 
Englert, Lukas 
Walter, Gary C 

Abstract

The synthesis of thiazoles and thiophenes starting from nitriles, via a modified Gewald reaction has been studied for a number of different substrates. 1,4-Dithiane-2,5-diol was used as the aldehyde precursor to give either 2-substituted thiazoles or 2-substituted aminothiophenes depending on the substitution of the α-carbon to the cyano group.

Description

Keywords

1,4-dithiane-2,5-diol, Gewald reaction, design of experiment (DOE), thiazole, thiophene

Journal Title

Beilstein J Org Chem

Conference Name

Journal ISSN

1860-5397
1860-5397

Volume Title

11

Publisher

Beilstein Institut