Photoredox-Induced Three-Component Azido- and Amino­tri­fluoro­methyla­tion of Alkenes

Abstract

We report herein a photoredox-catalyzed azido­trifluoro­methyla­tion of alkenes. Under the optimized conditions using [Ru­(bpy)<sub>3</sub>(PF<sub>6</sub>)<sub>2</sub>] as the photocatalyst and Umemoto’s reagent as the CF<sub>3</sub> source, a wide range of substituted styrenes as well as various activated and nonactivated alkenes can readily be difunctionalized, affording β-trifluoromethylated azides or amines in good yields

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