172291-73-5

Upstream product

• 98-88-4 benzoyl chloride 
• 3396-99-4 methyl α-D-galactopyranoside 
• 104477-38-5 methyl 2-O-benzyl-3,4-O-isopropylidene-6-O-(1-methoxy-1-methylethyl)-α-D-galactopyranoside 
• 81348-16-5 methyl 2-O-benzyl-α-D-galactopyranoside 
• 172291-72-4 methyl 3,4,6-tri-O-benzoyl-2-O-benzyl-α-D-galactopyranoside 

Downstream Products

• 172291-75-7 methyl O-(2,3-di-O-benzoyl-4,6-dideoxy-α-L-lyxo-hexopyranosyl)-(1<*>2)-3,4,6-tri-O-benzoyl-α-D-galactopyranoside 
• 172291-79-1 methyl O-(2-O-acetyl-3,4-di-O-benzoyl-α-L-rhamnopyranosyl)-(1<*>2)-3,4,6-tri-O-benzoyl-α-D-galactopyranoside 
• 172291-82-6 methyl O-(3,4-di-O-benzoyl-2,6-dideoxy-α-L-arabino-hexopyranosyl)-(1<*>2)-3,4,6-tri-O-benzoyl-α-D-galactopyranoside 
• 172291-80-4 methyl O-(3,4-di-O-benzoyl-α-L-rhamnopyranosyl)-(1<*>2)-3,4,6-tri-O-benzoyl-α-D-galactopyranoside 
• 172291-81-5 methyl O-(3,4-di-O-benzoyl-2-O-phenoxythiocarbonyl-α-L-rhamnopyranosyl)-(1<*>2)-3,4,6-tri-O-benzoyl-α-D-galactopyranoside 

Relevant academic research and scientific papers

Regioselective benzoylation of sugars mediated by excessive Bu2SnO: Observation of temperature promoted migration

Regioselective benzoylation of carbohydrates using an excess of dibutyltin oxide (Bu2SnO) at increased reaction temperatures has been developed for the synthesis of several glycoside benzoates with one or two free hydroxyl groups, including gal

Synthesis of specifically deoxygenated disaccharide derivatives of the Shigella dysenteriae type 1 O-antigen

The synthesis of methyl O-α-L-rhamnopyranosyl-(1 -> 2)-α-D-galactopyranosides specifically deoxygenated at position 2 (31), or 4 (21) of the rhamnopyranosyl residue was accomplished using methyl 3,4,6-tri-O-benzoyl-α-D-galactopyranoside (18) as the glycos