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    Transition-Metal-Free Cleavage of C–C Triple Bonds in Aromatic Alkynes with S<sub>8</sub> and Amides Leading to Aryl Thioamides

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    A novel transition-metal-free cleavage reaction of C–C triple bonds in aromatic alkynes with S<sub>8</sub> and amides furnishes aryl thioamides in moderate to excellent yields. The remarkable features of this thioamidation include the metal-free cleavage of C–C triple bond, mild reaction conditions, as well as wide substrate scope that is particularly compatible with some internal aromatic alkynes and acetamides
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