O-glycosylation

A chemical reaction that involves the transfer of a glycosyl group to an acceptor molecule.

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Facile O-glycosylation of glycals using Glu-Fe₃O₄-SO₃H, a magnetic solid acid catalyst
Related Chemicals
- n-octyl 3,4,6-tri-O-benzyl-2-deoxy-β-D-arabino-hexopyranoside
Effects of Glycosidation on Peptide Backbone Conformation
Related Chemicals
- O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl)-N^α-(fluoren-9-ylmethoxycarbonyl)-L-threonine pentafluorophenyl ester
Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf
Related Chemicals
- C₅₁H₄₃NO₁₂
Electron-deficient pyridinium salts/thiourea cooperative catalyzed O-glycosylation via activation of O-glycosyl trichloroacetimidate donors
Related Chemicals
- p-methoxybenzyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside

Yield NMR spectroscopy Catalyst Isolation Efficient Steric hindrance Mass spectrometry (MS) Conformation High-performance liquid chromatography (HPLC) Hydrogen bonding Thiourea Nuclear Magnetic Resonance (NMR) X-ray crystallography Reaction Conditions Circular Dichroism (CD) Catalytic Cycle Glycosidation Facile Activation Cooperative Catalysis Experimental terms Glycals N-Glycosylation Glycopeptide Isothermal titration calorimetry (ITC) Peptide Backbone Enzymatic Digestion Nuclear Overhauser Effect (NOE) Glycosyltransferase Anomeric Center

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