Issue 11, 2014

Iodine-catalysed oxidative cyclisation of acylhydrazones to 2,5-substituted 1,3,4-oxadiazoles

Abstract

An environmentally benign synthesis of 2,5-disubstituted 1,3,4-oxadiazoles has been developed starting from N-aroylhydrazones and N-acetylhydrazones at room or ambient temperature using a catalytic quantity of iodine in the presence of an aqueous hydrogen peroxide oxidant.

Graphical abstract: Iodine-catalysed oxidative cyclisation of acylhydrazones to 2,5-substituted 1,3,4-oxadiazoles

Supplementary files

Article information

Article type
Paper
Submitted
05 Sep 2013
Accepted
06 Nov 2013
First published
07 Nov 2013

RSC Adv., 2014,4, 5357-5362

Iodine-catalysed oxidative cyclisation of acylhydrazones to 2,5-substituted 1,3,4-oxadiazoles

G. Majji, S. K. Rout, S. Guin, A. Gogoi and B. K. Patel, RSC Adv., 2014, 4, 5357 DOI: 10.1039/C3RA44897E

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