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Synthetic Approach Toward Antibiotic Tunicamycins, 4. X-Ray Crystal Structure Analysis of a Higher-Carbon Nitro Sugar
10
Citations
9
References
1982
Year
Higher-carbon CarbohydrateGlycobiologyOrganic ChemistryHigher-carbon Nitro SugarPolysaccharideCarbohydrate-protein InteractionChemistryChemical BiologyMedicinal ChemistryStereoselective SynthesisBiochemistryAntimicrobial CompoundAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringChiral CentersNatural SciencesMicrobiologyMedicineSynthetic ChemistryNitro Sugar
Abstract A higher-carbon carbohydrate, a derivative of undecose has been synthesized by the potassium fluoride-catalyzed addition of a nitro sugar to a sugar aldehyde. The addition of methyl 5-de-oxy-2,3-O-isopropylidene-5-nitro-β-D-ribofuranoside to methyl 2-benzyloxycarbonylamino-2-deoxy-3,4-O-isopropylidene-α-D-galacto-dialdopyranoside-(1, 5) yielded a single diastereomer of the nitro undecose derivative. The absolute configuration of two chiral centers of the derivative has been established by the X-ray crystal structure analysis.
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