Copper-catalyzed olefinic C–H difluoroacetylation of enamides

Abstract

Copper-catalyzed olefinic difluoroacetylation of enamides via direct C–H bond functionalization using BrCF₂CO₂Et is reported for the first time. It constitutes an efficient radical-free method for the regioselective synthesis of β-difluoroester substituted enamides which exhibits broad substrate scope, and thus demonstrates its potent application in a late stage fluorination strategy.