1316822-87-3

Upstream product

• 501088-85-3 ethyl 2-amino-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside 
• 1147438-51-4 p-nitrophenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranoside 
• 83025-20-1 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranosyltrichloroacetimidate 
• 1316822-99-7 p-nitrophenyl 2-azido-2-deoxy-4,6-O-p-methoxybenzylidene-α-D-galactopyranoside 
• 235752-73-5 p-nitrophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside 
• 210418-04-5 C₁₂H₁₄N₄O₇ 
• 1316823-35-4 p-nitrophenyl 2-acetamido-4,6-di-O-benzoyl-2,3-N,O-carbonyl-2-deoxy-β-D-glucopyranosyl-(1->6)-2-azido-3-O-benzoyl-2-deoxy-α-D-galactopyranoside 
• 1316823-07-0 ethyl 2-acetamido-4,6-di-O-benzoyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside 
• 1316823-05-8 ethyl 2-amino-4,6-di-O-benzoyl-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside 
• 1316823-01-4 p-nitrophenyl 2-azido-3-O-benzoyl-2-deoxy-α-D-galactopyranoside 
• 1316823-00-3 p-nitrophenyl 2-azido-3-O-benzoyl-2-deoxy-4,6-O-p-methoxybenzylidene-α-D-galactopyranoside 
• 100-02-7 4-nitro-phenol 

Relevant academic research and scientific papers

Synthesis of mucin O-glycan core structures as their p-nitro- and p-aminophenyl glycosides

For the investigation of glycosidases, and for the construction of glycan arrays the p-nitrophenyl- and p-aminophenyl glycosides of mucin O-glycan core structures 1-7 and the 2,6-ST-antigen have been chemically synthesized using d-galactose as a precursor for GalNAc residues. GlcNAc residues have partly been introduced using a 4,6-di-O-benzoyl-2,3-N,O-oxazolidinone-protected donor, which allowed deprotection of the formed di- and tri-saccharides in one step using sodium methoxide.