Gold-Catalyzed Nucleophilic Ring-Opening Reaction of 2-Alkynylazetidines with Alcohols.
Tsukasa HirokaneTouya KariyaMisa TakataKenji MatsumotoMasahiro YoshidaPublished in: The Journal of organic chemistry (2022)
The reaction of 2-alkynylazetidines and alcohols with a gold catalyst is described. A variety of substituted δ-amino-α,β-unsaturated ketones were synthesized via gold-promoted nucleophilic attack of alcohols followed by ring-opening of azetidine ring.