220645-60-3

Upstream product

• 100-39-0 benzyl bromide 
• 220645-86-3 p-methylphenyl 4,6-O-benzylidene-1-thio-β-D-galactopyranoside 
• 1152-39-2 p-methylphenyl-1-thio-β-D-galactopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 100-52-7 benzaldehyde 

Downstream Products

• 1427297-46-8 methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranosyl-α(1→3)-4,6-O-benzylidene-2-O-benzyl-D-galactopyranosyl-α(1→4)-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 1427297-45-7 p-tolyl 2,3,4,6-tetra-O-benzyl-D-galactopyranosyl-α(1→3)-4,6-O-benzylidene-2-O-benzyl-thio-β-D-galactopyranoside 

Relevant academic research and scientific papers

Sub-stoichiometric reductive etherification of carbohydrate substrates and one-pot protecting group manipulation

In this study, we report a new reductive etherification procedure for protection of carbohydrate substrates and its application for one-pot preparation of glycosyl building blocks. The reported procedure features the use of polymethylhydrosiloxane (PMHS)

Programmable one-pot oligosaccharide synthesis

In an effort to develop a broadly applicable approach to the facile one- pot synthesis of oligosaccharides, the reactivity of a number of p- methylphenyl thioglycoside (STol) donors which are either fully protected or have one hydroxyl group exposed has b