Catalytic transformation of esters of 1,2-azido alcohols into α-amido ketones†
Abstract
The esters of 1,2-azido alcohols were transformed into α-amido ketones without external oxidants through the Ru-catalyzed formation of N–H imines with the liberation of N2 followed by intramolecular migration of the acyl moiety. A wide range of α-amido ketones were obtained, and one-pot transformation into the corresponding oxazoles (or a thiazole) was demonstrated.
- This article is part of the themed collection: Celebrating the 75th Anniversary of the Korean Chemical Society (KCS)