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The nephritogenic glycopeptide from rat glomerular basement membrane: synthesis of α-<scp>D</scp>-glucopyranosylamine derivatives
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1980
Year
GlomerulonephritisBioorganic ChemistryC Nmr SpectraBiochemistryGlycosylationMedicineNatural SciencesGlycobiologyPeptide ScienceMembrane BiologyProtecting GroupsPharmacologyCorresponding Glycosylamine DerivativesCarbohydrate-protein InteractionNephritogenic Glycopeptide
N-(L-β-aspartyl)-α-D-glucopyranosylamine has been prepared, as a model of a corresponding derivative possibly present in glomerular basement membrane of rats, by the condensation of α-ethyl benzyloxycarbonyl-L-aspartate with 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosylamine in the presence of diethylphosphorocyanidate. This was followed by hydrogenolysis, de-O-acetylation, and deethoxylation of the resulting 2,3,4,6-tetra-O-acetyl-N-(α-ethyl benzyloxycarbonyl-L-β-aspartyl)-α-D-glucopyranosylamine to remove the protecting groups. The 13 C nmr spectra of the corresponding glycosylamine derivatives are analyzed and discussed.