4.8 Article

Total synthesis of (-)-archazolid B

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 129, 期 29, 页码 8960-+

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AMER CHEMICAL SOC
DOI: 10.1021/ja0733033

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  1. NIGMS NIH HHS [R01 GM067636] Funding Source: Medline

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A highly convergent synthesis of archazolid B, a potent and highly selective V-ATPase inhibitor, is described. A relay ring-closing metathesis reaction was used to form the 24-membered macrocyclic lactone, whereas the sensitive cis-triene moiety of the archazolids was assembled with a modified Stille coupling.

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