Visible-light-induced radical trifluoromethylthiolation of N-(o-cyanobiaryl)acrylamides

Abstract

An efficient and general visible-light-mediated trifluoromethylthiolation of N-(o-cyanobiaryl)acrylamides has been successfully accomplished using N-trifluoromethylthiosaccharin as an effective source of SCF₃ radicals. The reaction was proposed to proceed via a domino radical trifluoromethylthiolation/cyano insertion/cyclization to afford the corresponding SCF₃-containing ring-fused phenanthridine derivatives in moderate to good yields.