Abstract
Trifluoromethanesulfenamide reagent, initially designed as electrophilic reagent, can be considered as a trifluoromethylthio anion source in presence of tetrabutylammonium iodide. Herein, we report the reaction of trifluoromethanesulfenamide with organoselenocyanates to prepare under mild conditions compounds bearing a new fluorinated group, namely SeSCF3.
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