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Studies on the Constiuents of Viburnum Species. Part XIII. Isolation and Absolute Structures of the Neolignan Glycosides with the Enantiometric Aglycones from the Leaves of Viburnum awabuki K. KOCH.
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1996
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Dihydrodehydrodiconiferyl Alcohol 4-O-β-d-glucopyranosidesBioorganic ChemistryBotanyGlycobiologyViburnum SpeciesNeolignan GlycosidesPhytochemicalGlycosylationAbsolute StructuresBiochemistryBioassay-guided IsolationCircular Dichroism DataBiomolecular EngineeringBiologyNatural SciencesMicrobiologyPhytochemistryMedicineCarbohydrate-protein Interaction
Two neolignan glycosides, dihydrodehydrodiconiferyl alcohol 4-O-β-D-glucopyranosides with the enantiometric aglycones (1 and 2), have been isolated from the leaves of Viburnum awabuki K. KOCH. These structures were identified by spectroscopic evidence and the absolute configurations of these compounds were elucidated on the basis of circular dichroism data.