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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
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