Issue 6, 2016

One pot synthesis of substituted imidazopyridines and thiazoles from styrenes in water assisted by NBS

Abstract

Heating of commercially available styrenes with NBS in water followed by reaction with 2-aminopyridines or thioamides afforded important heterocyclic scaffolds in a one pot procedure. The reaction proceeds via co-oxidant free, in situ formation of α-bromoketone using NBS as a bromine source as well as an oxidant followed by trapping with suitable nucleophiles to provide imidazopyridines and thiazoles.

Graphical abstract: One pot synthesis of substituted imidazopyridines and thiazoles from styrenes in water assisted by NBS

Supplementary files

Article information

Article type
Communication
Submitted
18 Nov 2015
Accepted
12 Dec 2015
First published
15 Dec 2015

Green Chem., 2016,18, 1455-1458

Author version available

One pot synthesis of substituted imidazopyridines and thiazoles from styrenes in water assisted by NBS

M. H. Shinde and U. A. Kshirsagar, Green Chem., 2016, 18, 1455 DOI: 10.1039/C5GC02771C

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