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Title: Synthesis of the C1-C13 tetraenoate subunit of the chivosazoles. Author: Paterson I, Kan SB, Gibson LJ. Journal: Org Lett; 2010 Aug 20; 12(16):3724-7. PubMed ID: 20704420. Abstract: Using a combination of asymmetric vinylogous Mukaiyama aldol and Stille cross-coupling reactions, an advanced polyene fragment of the chivosazoles was prepared in a highly stereocontrolled manner. This key C1-C13 pentaene subunit, featuring the conjugated (2E,4Z,6E,8Z)-tetraenoate motif and anti-configured C10 and C11 stereocenters of the chivosazoles, terminates in a (Z)-vinyl bromide for the planned cross-coupling to a northern hemisphere fragment.[Abstract] [Full Text] [Related] [New Search]