Sulfoxide Synthesis from Sulfinate Esters under Pummerer-like Conditions

A facile synthetic method of allyl sulfoxides by S -allylation of sulfinate esters through sulfonium intermediates has been developed without [3,3]-sigmatropic rearrangement and further Pummerer-type reactions of the resulting allyl sulfoxides. On the basis of the plausible reaction mechanism involving sulfonium salt intermediates, S-alkynylation and S-arylation were also accomplished.