42927-11-7

Upstream product

• 100-39-0 benzyl bromide 
• 78780-59-3 benzyl 3-O-allyl-β-D-galactopyranoside 
• 78727-75-0 Benzyl 3,6-di-O-Allyl-β-D-galactopyranoside 
• 4304-12-5 benzyl β-D-galactopyranoside 

Downstream Products

• 77777-81-2 benzyl 6-O-benzoyl-2,4-di-O-benzyl-β-D-galactopyranoside 
• 62447-55-6 Benzyl 2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 125084-92-6 benzyl 6-O-benzoyl-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-deoxy-β-D-arabino-hexapyranosyl)-β-D-galactopyranoside 
• 125084-91-5 benzyl 6-O-benzoyl-2,4-di-O-benzyl-(3,4,6-tri-O-acetyl-2-deoxy-2-isocyano-β-D-glucopyranosyl)-β-D-galactopyranoside 
• 125084-90-4 benzyl 6-O-benzoyl-2,4-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-deoxy-2-formamido-β-D-glucopyranosyl)-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

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