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• W2066881010 abstract "[structure: see text] The enantioselective synthesis of the enantiomer of the haterumalide NA methyl ester, a cytotoxic macrolide from an Okinawan sponge, was achieved from the threitol derivative in 26 steps. The key steps are the stereoselective construction of a chloroolefin unit and the intramolecular Reformatsky-type reaction. This synthesis revised the absolute stereochemistry of haterumalide NA." @default.
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• W2066881010 date "2003-02-26" @default.
• W2066881010 modified "2023-10-12" @default.
• W2066881010 title "Enantioselective Synthesis of 15-<i>e</i><i>pi</i>-Haterumalide NA Methyl Ester and Revised Structure of Haterumalide NA" @default.
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• W2066881010 doi "https://doi.org/10.1021/ol0341804" @default.
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