Issue 48, 2021

Electrochemical synthesis of 1,2,4-oxadiazoles from amidoximes through dehydrogenative cyclization

Abstract

A convenient and efficient method for the generation of the iminoxy radical through anodic oxidation was developed for the synthesis of 3,5-disubstituted 1,2,4-oxadiazoles from N-benzyl amidoximes. The transformation proceeds through 1.5-Hydrogen Atom Transfer (1,5-HAT) and intramolecular cyclization. The process features simple operation, mild conditions, broad substrate scope and high functional group compatibility, and provides a facile and practical way for the preparation of 1,2,4-oxadiazoles.

Graphical abstract: Electrochemical synthesis of 1,2,4-oxadiazoles from amidoximes through dehydrogenative cyclization

Supplementary files

Article information

Article type
Paper
Submitted
18 Oct 2021
Accepted
19 Nov 2021
First published
25 Nov 2021

Org. Biomol. Chem., 2021,19, 10611-10616

Electrochemical synthesis of 1,2,4-oxadiazoles from amidoximes through dehydrogenative cyclization

C. Jiang, M. Li, L. Xu, Y. Yi, J. Ye and A. Hu, Org. Biomol. Chem., 2021, 19, 10611 DOI: 10.1039/D1OB02040D

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