“Syn-Effect” in the Desulfonylation Reaction ofα,α-Dialkylated (E)-Allylic Sulfones

It was found that the desulfonylation reaction of α,α-dialkylated (E)-allylic sulfones with a base preferentially affords the sterically unfavorable (Z)-alkadienes. The relative degree of the “syn-effect”, which is herein defined as an effect which stabilizes the syn-conformation, leading to (Z)-products, in the transition state against the steric hindrance, was revealed for various substituents at the δ-position of the (E)-allylic sulfones to be as follows: RO– >> CH3– > RS– > –CH2– > (CH3)2CH– >> (CH3)3C– > C6H5–. This finding is in accord with a previously found tendency in the conversion of (E)-vinylic sulfones to the corresponding allylic sulfones under basic conditions.