Data di Pubblicazione:
2007
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.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Enantioselective synthesis; Prostanoids; Metabolites
Elenco autori:
Porta, Alessio; Re, Savino; Zanoni, Giuseppe; Vidari, Giovanni
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