A visible-light-induced, catalyst-free radical cross-coupling cyclization of diselenides or disulfides with N -allylbromodifluoroacetamide has been developed. This developed protocol exhibits good functional group tolerance and affords a variety of 4-thio- and 4-seleno-substituted 3,3-difluoro-γ-lactams in moderate to good yields. Based on control experiments, a plausible radical–radical cross-coupling pathway is proposed.
No takes yet. Share an insight, caveat, or question.
Ye et al. (2020) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: