78727-75-0

Upstream product

• 78780-59-3 benzyl 3-O-allyl-β-D-galactopyranoside 
• 106-95-6 allyl bromide 
• 4304-12-5 benzyl β-D-galactopyranoside 

Downstream Products

• 63070-10-0 benzyl 3,6-di-O-allyl-2,4-di-O-benzyl-β-D-galactopyranoside 
• 212198-17-9 Trifluoro-methanesulfonic acid (2R,3R,4S,5S,6R)-4-allyloxy-6-allyloxymethyl-2-benzyloxy-5-trifluoromethanesulfonyloxy-tetrahydro-pyran-3-yl ester 
• 42927-11-7 benzyl 2,4-di-O-benzyl-β-D-galactopyranoside 
• 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

Novel synthetic approaches to manβ1-4GLCNAc and LeX units from N-acetyllactosamine

Regioselective protection of N-acetyllactosamine with triphenylmethyl (trityl) and pivaloyl groups afforded the corresponding 3, 2′, 4′-tri- and 2′,4′-dihydroxyl derivatives in a few steps, respectively; these derivatives were used efficiently for the syntheses of the title compounds from N-acetyllactosamine in 46% (7 steps) and 19% (8 steps) overall yields, respectively.

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