Publication | Open Access
Assignment of anomeric configuration and identification of carbohydrate residues by <sup>13</sup>C nmr. 1. Galacto- and glucopyranosides and furanosides
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Citations
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References
1980
Year
Bioorganic ChemistryBiochemistryNatural SciencesC NmrGlycobiologyStructural ConfigurationMolecular BiologyPolysaccharideCarbohydrate ResiduesAnomeric ConfigurationMolecular RecognitionMedicineCarbohydrate-protein InteractionStructural BiologyBiomolecular EngineeringGlycosylation
A 13 C nmr analysis method is described for the identification of carbohydrate residues in galactosides and glucosides. This method reveals the capability of 13 C nmr to distinguish the difference in structural configuration of these carbohydrate residues. Not only can the anomeric configuration be assigned, the furanyl and pyranyl nature of the ring is concomitantly determined. This method is consistent for all reported 13 C nmr spectra of nonaromatic galactosides and glucosides.
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