Demonstrates high yield trifluoromethylation and sulfuration in alkenes, indicating new reactivity pathways.
Under photocatalytic conditions, a novel and highly reactive trifluoromethylthiolation reagent, S-aryl trifluoromethanesulfonothioate (TTSA), reacted with various unactivated alkenes to produce sulfurized and trifluoromethylated derivatives in high yields. Furthermore, a series of experimental studies were conducted, such as radical trapping experiments, scrambling experiments, cyclic voltammetry (CV) measurements, Stern–Volmer analysis, and light on/off control experiments, to support the photocatalytic reduction quenching cycle reaction pathway.
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