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Title: Total synthesis of (-)-reveromycin a. Author: El Sous M, Ganame D, Tregloan PA, Rizzacasa MA. Journal: Org Lett; 2004 Aug 19; 6(17):3001-4. PubMed ID: 15330668. 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.[Abstract] [Full Text] [Related] [New Search]