108739-99-7

Upstream product

• 108672-19-1 methyl 2-O-acetyl-4,6-O-benzylidene-3-O-<(methylthio)thiocarbonyl>-β-D-galactopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 108672-18-0 methyl 4,6-O-benzylidene-3-O-<(methylthio)thiocarbonyl>-β-D-galactopyranoside 
• 1824-94-8 methyl beta-D-galactopyranoside 
• 71117-36-7 methyl 4,6-O-(S)-benzylidene-β-D-galactopyranoside 

Downstream Products

• 108740-00-7 methyl 4,6-O-benzylidene-3-deoxy-β-D-xylo-hexopyranoside 
• 108672-20-4 methyl 2,6-di-O-benzyl-3-deoxy-β-D-xylo-hexopyranoside 
• 108740-01-8 methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-β-D-xylo-hexopyranoside 

Relevant academic research and scientific papers

Building Units of Oligosaccharides, CIX. - Synthesis of Modified Oligosaccharides of N-Glycoproteins for Substrate Specificity Studies of N-Acetylglucosaminyltransferase I

A series of modified derivatives of the trisaccharide octyl α-D-Man(1-->3)-6)>-β-D-Man were synthesized for substrate specificity studies of N-acetylglucosaminyltransferase I (GlcNAc-T I).The hydroxyl groups at C-3, C-4 and C-6 of the α(1-->3

SYNTHETIC RECEPTOR ANALOGUES: PREPARATION OF THE 3-O-METHYL, 3-C-METHYL, AND 3-DEOXY DERIVATIVES OF METHYL 4-O-α-D-GALACTOPYRANOSYL-β-D-GALACTOPYRANOSIDE (METHYL β-D-GALABIOSIDE)

Methyl β-D-galactopyranoside was transformed into methyl 2-O-benzyl- (5, 24percent) and 2-O-benzyloxymethyl-4,6-O-benzylidene-β-D-galactopyranoside (8, 60percent) in two and four steps respectively.Compounds 5 and 8 were then transformed into the correspo