Enantioselective Total Synthesis of Otteliones A and B
收藏NIAID Data Ecosystem2026-03-06 收录
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https://figshare.com/articles/dataset/Enantioselective_Total_Synthesis_of_Otteliones_A_and_B/2780626
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资源简介：
Enantioselective total synthesis of otteliones A and B was accomplished. The key steps are radical cyclization of an alpha-iodoketone to construct the cis-hydrindanone skeleton and Suzuki−Miyaura coupling to incorporate the aromatic group. (+)-Ottelione A was converted to (−)-ottelione B on treatment with NaOH in THF.
创建时间：
2016-02-25
