This method shows efficient carbonylative cyclization of bromodifluoroacetamides with arylboronic acids, suggesting broad applications in medicinal chemistry.
A nickel-catalyzed radical cyclization/carbonylation reaction of bromodifluoroacetamides with arylboronic acids has been explored. This strategy allows for the synthesis of δ-lactams bearing both gem-difluoro and carbonyl groups through a sequential single-electron transfer, 6-exo-trig cyclization, and carbonyl insertion process. This method proceeds under mild reaction conditions with good functional group compatibility, enabling the preparation of various structurally diverse δ-lactams that might have further applications in medicinal chemistry.
No takes yet. Share an insight, caveat, or question.
Ma et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: