Australian Journal of Chemistry · 1971 · 11 citations · 0 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySteroid BiochemistryAroma CompoundsAromatic PlantsFlavonoid BiosynthesisHeterocyclic ChemistryMetabolite IdentificationTerpenoid Biosynthesis
Chloroform extraction of Olearia heterocarpa S. T. Blake has yielded a new diterpene dilactone, olearin, the known flavone, xanthomicrol, an unknown C27H42O3 hydroxy acid, and a mixture of long-chain (approx. C50) esters. On chemical and spectroscopic evidence olearin (1) has been shown to possess a rearranged enantio-labdane skeleton of the type displayed by the cascarillins. Correlation of olearin with a diterpene of known stereochemistry has defined the absolute con- figuration at all but one centre.