Electrochemically driven regioselective construction of 4-sulfenyl-isochromenones from o -alkynylbenzoates and diaryl disulfides.

Herein, we report a convenient and environmentally friendly electrochemical technique that enables the regioselective construction of 4-sulfenyl-1 H -isochromen-1-ones using readily available precursors such as o -alkynyl benzoates and diaryl disulfides. This electrochemical process has been accomplished through constant current electrolysis in an undivided cell under external acid, catalyst, oxidant, or metal-free conditions. Owing to this protocol's mild reaction conditions, the products are obtained in good to very good yields, demonstrating a broad substrate scope and functional group tolerance.