Synthesis of Iso-agatharesinol

Abstract
A highly diastereoselective deprotonation of a benzylic sulfonium salt A and a stereo­specific 1,2-metallate rearrangement (D to E) are key steps in a short synthesis of (+)-iso­agatharesinol, a nor-lignan of Asparagus gobicus with potent cytotoxic activity against human ovarian carcinoma and human hepatoma.