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Updated: Sep 15, 2025

Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
Formal total synthesis of (±)-liphagal
Sora Yotsui1, Takehiko Yoshimitsu1
1Division of Pharmaceutical Sciences, Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushimanaka, Kita-ku, Okayama 700-8530, Japan. yoshimit@okayama-u.ac.jp.
None:
A formal total synthesis of (±)-liphagal is reported. The key features of the synthetic route include a novel copper/1,2,4-benzenetriol-promoted hydroxybenzofuran formation from an alkynylquinone via an organic redox process, a silver(I)-catalyzed cationic seven-membered ring construction, and a stereoconvergent synthesis of the desired diastereomer with the natural relative configuration through unsaturation followed by stereoselective hydrogenation.
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