A protocol for the synthesis of trisubstituted furans via phosphoric acid‐catalyzed regioselective cascade cyclization/amination of para ‐quinone methides ( p ‐QMs) with β ‐ketodinitriles has been disclosed for the first time. Various kinds of p ‐QMs and β ‐ketodinitriles can effectively produce the desired polysubstituted furan derivatives in 64–95% yields, demonstrating high atomic economy and their application in the construction of polysubstituted furan heterocycles. Preliminary biological activity assay suggests that these furans have potential anticancer activities.
No takes yet. Share an insight, caveat, or question.
Fan et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: