Zn(OTf)2‑Catalyzed Phosphinylation of Propargylic Alcohols: Access to γ‑Ketophosphine Oxides

The first facile and efficient Zn­(OTf)2-catalyzed direct coupling of unprotected propargylic alcohols with arylphosphine oxides has been developed, affording a general, one-step approach to access structurally diverse γ-ketophosphine oxides via sequential Meyer–Schuster rearrangement/phospha-Michael reaction along with new C­(sp3)P and CO bond formations, operational simplicity, and complete atom economy under ligand-free and base-free conditions.