Cyclization of Carbonyl Groups onto Alkynes upon Reaction with IPy₂BF₄ and Their Trapping with Nucleophiles: A Versatile Trigger for Assembling Oxygen Heterocycles

Abstract

Iodonium ions liberated from bis(pyridine)iodonium(I) tetrafluoroborate react with ortho-alkynyl-substituted carbonyl compounds and different nucleophiles to give valuable iodinated heterocycles at room temperature, through a new and metal-free reaction sequence. Interestingly, the nature of the nucleophile can be widely modified, and not only alcohols but also several carbon-based nucleophiles can be nicely used.