Australian Journal of Chemistry · 1969 · 33 citations · 0 references
PharmacyBiochemistryChemistryNatural Product BiosynthesisOrganic ChemistrySteroid BiochemistryFlavonoid BiosynthesisHeterocyclic ChemistryPhenylpropanoid BiosynthesisTerpenoid BiosynthesisFlavonoid Metabolism
Several 2,2-dimethylchromene derivatives, including the natural flavonoids scandenin and lonchocarpic acid, have been reduced by lithium in ammonia to o-isopentenylphenols. Several hydroxyisopropyldihydrobenzofurans can similarly be reduced, and one was converted by reaction with N-bromosuccinimide into a benzofuran derivative lacking the isopropyl group. Alkylations of catechol and aesculetin with isoprene dibromide were examined, and in the latter case resulted in what is probably (±)-obliquin.