Enantioselective Synthesis of (−)-Sclerophytin A by a Stereoconvergent Epoxide Hydrolysis
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https://figshare.com/articles/dataset/Enantioselective_Synthesis_of_Sclerophytin_A_by_a_Stereoconvergent_Epoxide_Hydrolysis/2710366
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资源简介：
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：
2010-11-24
