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Enantioselective synthesis of preclavulone A and its methyl ester
Authors:Alessio Porta
Institution:Department of Organic Chemistry, University of Pavia, Viale Taramelli, 10, 27100 Pavia, Italy
Abstract:A highly enantioselective synthesis of the (8S,12S)-enantiomer of preclavulone A and its methyl ester is described featuring the Julia protocol for installing the (Z)-double bond in the lower chain. This procedure is suitable for the preparation of labeled preclavulone analogues for biosynthetic studies on marine clavulones.
Keywords:Preclavulone A  Marine clavulones  Enantioselective synthesis  Julia olefination
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