摘要

A mild and efficient protocol for photoredox-catalyzed azidofluoroalkylation of simple alkenes is described with readily available fluoroalkyl iodides. This method allows for a direct and regioselective formation of C-R-F and C-N-3 bonds from the C=C moiety. A variety of fluoroalkyl groups including the CF3 group can be selectively introduced to olefins to afford a series of,beta-fluoroalkylated azides.