616861-57-5

Upstream product

• 100-39-0 benzyl bromide 
• 616861-56-4 3,4,6-tri-O-acetyl-α-D-galactopyranose-1,2-O-diyl allyl orthoacetate 
• 25878-60-8 D-galactose pentaacetate 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 

Downstream Products

• 616861-58-6 allyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 148926-02-7 2-O-benzoyl-3,4,6-tri-O-benzyl-D-galactopyranose 
• 162466-65-1 allyl 3,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 616861-59-7 allyl 2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 616861-62-2 allyl 2-O-p-methoxybenzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 616861-63-3 allyl 2-O-p-nitrobenzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 616861-60-0 2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl trichloroacetimidate 
• 616861-61-1 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-galactopyranosyl trichloroacetimidate 
• 616861-67-7 2-O-p-methoxybenzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl trichloroacetimidate 
• 616861-65-5 2-O-p-methoxybenzoyl-3,4,6-tri-O-benzyl-α-D-galactopyranosyl trichloroacetimidate 
• 616861-68-8 2-O-p-nitrobenzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl trichloroacetimidate 
• 616861-66-6 2-O-p-nitrobenzoyl-3,4,6-tri-O-benzyl-α-D-galactopyranosyl trichloroacetimidate 
• 616861-53-1 methyl (3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->2)-(allyl 3,4-di-O-methoxymethyl-β-D-glucopyranosid)uronate 
• 616861-51-9 methyl (2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->2)-(allyl 3,4-di-O-methoxymethyl-β-D-glucopyranosid)uronate 

Relevant academic research and scientific papers

Carboxymethylglycoside lactones (CMGLs): structural variations on the carbohydrate moiety

New glucose and galactose based bicyclic lactones, with variations in the anomeric configuration, the protecting groups (acetyl or benzyl) and the furanosyl or pyranosyl rings were synthesized from allyl glycosides and used for the preparation of a series

Synthesis of the trisaccharide portion of soyasaponin βg: Evaluation of a new glucuronic acid acceptor

The synthesis of the trisaccharide portion of soyasaponin βg was successfully achieved using a new glucuronic acid acceptor: methyl 1-O-allyl-3,4-di-O-methoxymethyl-β-D-glucuronate (9). This compound and methyl 1-O-allyl-3,4-di-O-tert-butyldimethylsilyl-β