Abstract
Abstract Reaction of bistrifluoromethylaminosulphenyl chloride with acyclic and alicyclic hydrocarbon olefins at −78 °C in the dark affords 1:1 adducts of type in high yield. Treatment of diaryl disulphides with the N -bromo-amine (CF3)2NBr or of benzenesulphenyl chloride with the mercurial [(CF3)2N]2Hg provide convenient routes to bistrifluoromethylaminosulphenylarenes.
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