Manganese(I) Catalyzed Alkenylation of Phosphine Oxides Using Alcohols with Liberation of Hydrogen and Water

Abstract

Herein, a catalytic cross-coupling of methyldiphenylphosphine oxide with arylmethyl alcohols leading to the alkenylphosphine oxides is reported. A manganese pincer catalyst catalyzes the reactions, which provides exclusive formation of <i>trans</i>-alkenylphosphine oxides. Mechanistic studies indicate that reactions proceed via aldehyde intermediacy and the catalyst promotes the C═C bond formation. Reactions are facilitated by dearomatization, and aromatization metal-ligand cooperation operates in catalyst. Use of abundant base metal catalyst and formation of water and H₂ as the only byproducts make this catalytic protocol sustainable and environmentally benign.