Journal of the American Chemical Society · 2002 · 118 citations · 11 references
Natural SciencesChemistryToxicologyAquatic ToxicologyMarine ToxicologyOrganic ChemistryMarine BiotoxinsOrganic SynthesisBiological Activity FeaturesDinoflagellate ToxinsGambierdiscus ToxinsMarine Toxins As Drug Leads
The convergent total synthesis of gambierol (1) is described. The octacyclic ether framework of 1 was constructed via the intramolecular allylation of alpha-chloroacetoxy ether followed by ring-closing metathesis. A modified Stille coupling was successfully applied to the synthesis of the triene side chain.
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