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A chiral thulium(III)-catalyzed sulfur-conjugation addition reaction of dialkynylphosphine oxides to construct P-stereogenic centers has been developed. Dialkynylphosphine oxides bearing aryl, alkyl, alkenyl substitution at the alkyne terminus position were tolerated under the reaction conditions. The corresponding P,S-containing compounds were obtained in moderate to good yields (up to 92% yield) with high Z/E ratios and enantioselectivities (up to >95/5 Z/E and 97% ee), which could be transformed into versatile optically active phosphine oxide derivatives. X-ray single crystal structures of chiral N,N′-dioxides with rare-earth metal triflates revealed how the metal center and ligand structure affect the enantioselectivity.
Zhang et al. (Wed,) studied this question.