63070-10-0

Upstream product

• 4304-12-5 benzyl β-D-galactopyranoside 
• 69359-15-5 benzyl 3,6-di-O-allyl-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 3458-28-4 D-Mannose 
• 100-51-6 benzyl alcohol 
• 15548-45-5 (2S,3S,4S,5S,6R)-2-benzyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 
• 78780-59-3 benzyl 3-O-allyl-β-D-galactopyranoside 
• 78727-75-0 Benzyl 3,6-di-O-Allyl-β-D-galactopyranoside 

Downstream Products

• 69401-46-3 benzyl 2,4-di-O-benzyl-α-D-mannopyranoside 
• 62447-55-6 Benzyl 2,4,6-tri-O-benzyl-β-D-galactopyranoside 

Relevant academic research and scientific papers

Method for producing oligosaccharide, and novel oligosaccharide and pharmaceutical composition containing the same

Oligosaccharides including those usable as anti-inflammatory agent or anti-allergy agent, represented by the following general formula (3): wherein R10and R11each independently represent a hydrogen atom or —SO3M where M re

Synthesis of O-β-D-Galactopyranosyl-(1->4)-O-2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-D-mannose, a Postulated Trisaccharide of Human Erythrocyte Membrane Sialoglycoprotein

Monoallylation of tributylstannylated benzyl 6-O-trityl-α-D-mannopyranoside (3) was efficiently catalysed by tetrabutylammonium bromide to give the 3-O- (4) and 2-O- (5) allyl ethers in 62 and 15percent yields, respectively.Compound (4) was converted into

A Mild Procedure for the Regiospecific Benzylation and Allylation of Polyhydroxy-compounds via their Stannylene Derivatives in Non-polar Solvents

The reactions of benzyl and allylbromides on the stannylene derivatives of polyhydroxy-compounds, which normally proceed only at insignificant speed in refluxing benzene solution, are greatly accelerated in the presence of quaternary ammonium halides.Thes