Enantioselective Synthesis of (−)-Sclerophytin A by a Stereoconvergent Epoxide Hydrolysis
收藏NIAID Data Ecosystem2026-03-06 收录
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The cytotoxic natural product (−)-sclerophytin A was constructed in 13 steps from geranial. Highlights from the synthesis are a stereoselective Oshima−Utimoto reaction, a Shibata−Baba indium-promoted radical cyclization, and a novel stereoconvergent epoxide hydrolysis.
创建时间：
2016-02-24
