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• W4231265825 abstract "The unique structural features of the cytotoxic marine macrolide (−)-amphidinolide E make it an intriguing synthetic target. Its total synthesis has now been completed by employing a radical cyclization of a β-alkoxy acrylate to form the oxolane ring, a Kocienski–Julia olefination to create the E CC bond, and a lactonization reaction to close the macrocyclic ring." @default.
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• W4231265825 date "2006-11-27" @default.
• W4231265825 modified "2023-10-18" @default.
• W4231265825 title "Total Synthesis of (−)-Amphidinolide E" @default.
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• W4231265825 doi "https://doi.org/10.1002/anie.200603363" @default.
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