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Structures of the natural products blumenols A, B, and C
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1972
Year
Blumenols ABioorganic ChemistryEngineeringChemical CompositionAbscisic AcidMolecular BiologyOrganic ChemistryChemistryPodocarpus BlumeiStructure ElucidationNatural ProductsStereoselective SynthesisNatural Products ChemistryBiochemistryNatural MaterialsNatural Product SynthesisEnantioselective SynthesisNatural SciencesPhytochemistrySynthetic Chemistry
Blumenols A, B, and C, new compounds from Podocarpus blumei, are shown to have structures (1), (2), and (3), respectively, with the opposite stereochemistry to that of abscisic acid (4) at the ring chiral centre.