Issue 76, 2015

Azide–acetonitrile “click” reaction triggered by Cs2CO3: the atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles

Abstract

Medicinally important 5-amino-1,2,3-triazoles were synthesized using a novel Cs2CO3-catalyzed azide–acetonitrile[3 + 2]-cycloaddition. Aryl azides and aryl acetonitriles were employed in this transformation resulting in excellent yields with high regioselectivity.

Graphical abstract: Azide–acetonitrile “click” reaction triggered by Cs2CO3: the atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles

Supplementary files

Article information

Article type
Communication
Submitted
25 Jun 2015
Accepted
13 Jul 2015
First published
13 Jul 2015

RSC Adv., 2015,5, 62062-62066

Azide–acetonitrile “click” reaction triggered by Cs2CO3: the atom-economic, high-yielding synthesis of 5-amino-1,2,3-triazoles

P. M. Krishna, D. B. Ramachary and S. Peesapati, RSC Adv., 2015, 5, 62062 DOI: 10.1039/C5RA12308A

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