Copper(II) Triflate‐Catalyzed Nucleophilic Substitution of Propargylic Acetates with Enoxysilanes. A Straightforward Synthetic Route to Polysubstituted Furans

Abstract A novel and efficient procedure for the synthesis of γ‐alkynyl ketones by the nucleophilic substitution of propargylic acetates with enoxysilanes in the presence of a catalytic amount of Copper(II) triflate, has been developed. The substitution reaction can be followed by a 4‐toluenesulfonic acid‐catalyzed cyclization without purification of the γ‐alkynyl ketone intermediates, offering a straightforward synthetic route to polysubstituted furans.