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We report herein a photoredox-catalyzed azidotrifluoromethylation of alkenes. Under the optimized conditions using Ru(bpy)3(PF6)2 as the photocatalyst and Umemoto's reagent as the CF3 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.
Dagousset et al. (Thu,) studied this question.
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