Unusual Regioselective C–H Difluoroalkylation of Heteroarenes under Photoredox Catalysis

We disclose a new general strategy for the site-selective difluoroalkylation of nonprefunctionalized heteroarenes, such as quinoxaline at the C-8 position, and benzothiadiazole, benzoxadiazole, and benzothiazole at the C-4 position via consecutive organophotoredox-catalyzed radical–radical cross-coupling and base-assisted hydrogen abstraction reactions. The current methodology represents a site-selective direct difluoroalkylative strategy to allow broad functional group tolerance and a wide substrate scope in good to excellent yields. Careful experimental investigations and detailed DFT calculations revealed the exact site-selectivity of the heteroarenes and a possible mechanistic pathway.