Issue 26, 2020

Palladium-catalyzed synthesis of 5-amino-1,2,4-oxadiazoles via isocyanide insertion

Abstract

A convenient and efficient palladium-catalyzed approach has been developed for the synthesis of 5-amino-1,2,4-oxadiazoles from amidoximes and isocyanides. Various 5-amino-1,2,4-oxadiazoles were obtained in moderate to high yields under mild conditions. The key to the success of this strategy involves new C–N bond and C–O bond formation via palladium-catalyzed isocyanide insertion.

Graphical abstract: Palladium-catalyzed synthesis of 5-amino-1,2,4-oxadiazoles via isocyanide insertion

Supplementary files

Article information

Article type
Communication
Submitted
27 May 2020
Accepted
17 Jun 2020
First published
18 Jun 2020

Org. Biomol. Chem., 2020,18, 4936-4940

Palladium-catalyzed synthesis of 5-amino-1,2,4-oxadiazoles via isocyanide insertion

X. Wang, J. Fu, J. Xie, Q. Teng, H. Tang and Y. Pan, Org. Biomol. Chem., 2020, 18, 4936 DOI: 10.1039/D0OB01092H

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