Publication | Open Access
Synthesis of <i>C</i>‐Glycopeptides via Free Radical Addition of Glycosyl Bromides to Dehydroalanine Derivatives
74
Citations
15
References
1992
Year
Free Radical AdditionBioorganic ChemistryEngineeringNonnatural C-glycopeptidesGlycobiologyMolecular BiologyOrganic ChemistryPolysaccharideChemical BiologyType 1Medicinal ChemistryDehydroalanine DerivativesGlycosylationBiochemistryReaction StepNatural Product SynthesisBiomolecular EngineeringGlycosyl BromidesNatural SciencesPeptide LibraryPeptide SynthesisCarbohydrate-protein Interaction
In only one reaction step, nonnatural C-glycopeptides of type 1 can be obtained (see right, (S) form). This new class of molecules has remarkable properties; their high chemical stability recommends them as potential glycosidase inhibitors. The absolute configuration of the C-glycopeptides can be elucidated with NMR spectroscopy and molecular dynamics calculations. (R1,R2 = H, OAc, sugar; R3,R4 = protecting group.)
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