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- W3143204216 abstract "The asymmetric total synthesis of (−)-reveromycin A is described. The key steps involved a Lewis acid catalyzed inverse electron demand hetero-Diels−Alder reaction followed by hydroboration/oxidation to afford the spiroketal core 4 in a highly stereoselective manner and introduction of the C18 hemisuccinate by high-pressure acylation." @default.
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- W3143204216 date "2004-07-22" @default.
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- W3143204216 title "Total Synthesis of (−)-Reveromycin A" @default.
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- W3143204216 doi "https://doi.org/10.1021/ol048811l" @default.
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