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

Org Biomol Chem. 2020 Jul 8;18(26):4936-4940. doi: 10.1039/d0ob01092h.

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.

Publication types

  • Research Support, Non-U.S. Gov't