Publication Date:
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.
Iris type:
1.1 Articolo in rivista
Keywords:
Enantioselective synthesis; Prostanoids; Metabolites
List of contributors:
Porta, Alessio; Re, Savino; Zanoni, Giuseppe; Vidari, Giovanni
Published in: