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- W2039779966 abstract "Abstract The stereoselective total synthesis of Ieodomycin A and B, bioactive secondary metabolites from marine sources with potent anti-microbial activity was achieved starting from commercially available geranial. The key steps involved in the synthetic sequence of Ieodomycin A and B are the Sharpless asymmetric epoxidation, the formation of a β-ketoester, and the 1,3- anti reduction. The synthesis of C-3 epimer of Ieodomycin A and B was also accomplished in good yields." @default.
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- W2039779966 date "2013-06-01" @default.
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- W2039779966 title "Stereoselective total synthesis of Ieodomycin A and B" @default.
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- W2039779966 doi "https://doi.org/10.1016/j.tetasy.2013.05.002" @default.
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