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• W2123128875 abstract "Sweet success: The classical approach to macrolide antibiotics involves a macrocyclization followed by the introduction of the carbohydrate residue(s). Now for the first time, a glycosylated seco-acid (see scheme, left) was cyclized to give an intermediate that was converted into a naturally occurring macrolide, as exemplified by the synthesis of erythromycin B (right)." @default.
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• W2123128875 date "2003-07-16" @default.
• W2123128875 modified "2023-10-17" @default.
• W2123128875 title "An Abiotic Strategy for the Enantioselective Synthesis of Erythromycin B" @default.
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• W2123128875 doi "https://doi.org/10.1002/anie.200351136" @default.
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