Thioethers as Dichotomous Electrophiles for Site‐Selective Silylation via C−S Bond Cleavage

The development of aryl alkyl sulfides as dichotomous electrophiles for site‐selective silylation via C−S bond cleavage has been achieved. Iron‐catalyzed selective cleavage of C(aryl)−S bonds can occur in the presence of β‐diketimine ligands, and the cleavage of C(alkyl)−S bonds can be achieved by t‐BuONa without the use of transition metals, resulting in the corresponding silylated products in moderate to excellent yields. Mechanistic studies suggest that Fe−Si species may undergo metathesis reactions during the cleavage of C(aryl)−S bonds, while silyl radicals are involved during the cleavage of C(alkyl)−S bonds. The development of aryl alkyl sulfides as dichotomous electrophiles for the site‐selective silylation via C−S bond cleavage has been achieved. The iron‐catalyzed selective cleavage of C(aryl)−S bonds can occur in the presence of β‐diketimine ligands, while the cleavage of C(alkyl)−S bonds can be achieved by t‐BuONa without the use of any transition metal, resulting in the corresponding silylated products with high efficiency.