Abstract

Optically active (E,S)-γ-hydroxy-α,β-unsaturated sulfones and (S)-Iµ-hydroxy-(E,E)-α,γ-dienyl sulfones have been prepared in a one-pot dehydration procedure from β,γ-dihydroxy sulfones and δ,Iµ-dihydroxy allyl, sulfones, respectively, via an elimination reaction of the corresponding cyclic sulfites or carbonates formed in situ by treatment with thionyl chloride or carbonyldiimidazole.

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