This novel synthetic method constructs heterocycle and alkylidenebutenolide units, indicating effective one-pot transformations.
A novel palladium-catalyzed cascade reaction process for the diverse synthesis of heterocycle-containing γ-alkylidenebutenolide frameworks has been developed. Using this protocol, γ-alkylidenebutenolide and δ-heterocycle units can be constructed simultaneously through one-pot multiple C–C/C–O bond formation of different iodoaryl-substituted alkenes with cyclopropenones, leading to nine types of heterocycle-containing γ-alkylidenebutenolides in generally acceptable yields. The advantage of this work is also featured by its gram-scale preparation, further diverse transformations, and good in vitro antitumor activities of the highly valuable and modifiable synthetic products.
No takes yet. Share an insight, caveat, or question.
Yang et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: