73108-30-2

Upstream product

• 73108-28-8 benzyl 2,6-O-benzyl-3,4-di-O-isopropylidene-β-D-galactopyranoside 
• 14897-51-9 Benzyl 3,4-O-isopropylidene-β-D-galactopyranoside 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 4304-12-5 benzyl β-D-galactopyranoside 

Downstream Products

• 115216-32-5 benzyl-2,6-di-O-benzyl-3-O-(3,4,6-tri-O-acetyl-2-azido-2-desoxy-β-D-galactopyranosyl)-β-D-galactopyranosid 
• 62420-56-8 benzyl 2,6-di-O-benzyl-endo-3,4-O-benzylidene-β-D-galactopyranoside 
• 96520-15-9 benzyl O--(2-3)-2,6-di-O-benzyl-β-D-galactopyranoside 
• 96520-16-0 benzyl O--(2-3)-2,6-di-O-benzyl-β-D-galactopyranoside 
• 73960-72-2 methyl-2,3-didehydro-4,7,8,9-tetra-O-acetyl-N-acetylneuraminate 
• 113473-47-5 C₄₆H₅₃NO₁₇ 
• 74801-02-8 benzyl 2,6-di-O-benzyl-3-O-trityl-β-D-galactopyranoside 
• 76637-92-8 benzyl 3-O-benzoyl-2,6-di-O-benzyl-β-D-galactopyranoside 
• 102854-32-0 Benzyl-2,6-di-O-benzyl-3,4-O-(1-ethoxyethyliden)-β-D-galactopyranosid 
• 255876-09-6 C₃₅H₃₄O₇S 
• 220449-91-2 benzyl 2,6-di-O-benzyl-3,4-O-sulfuryl-β-D-galactopyranoside 

Relevant academic research and scientific papers

Regioselective removal of the anomeric O-benzyl from differentially protected carbohydrates

A mild, regioselective deprotection of the anomeric O-benzyl from multi-functionally protected carbohydrates via catalytic transfer hydrogenation is described. The protocol is tolerant of O-benzyl and O-benzylidene protections at non-anomeric positions, g

TOTAL SYNTHESIS OF SIALOSYLCEREBROSIDE, GM4

Desribed are total syntheses of O--(2->3)-O-β-D-galactopyranosyl-(1->1)-(2S,3R,4E)-2-N-tetracosanoylsphingenine, O--(2->3)-O-α-D-galactopyranosyl-(1->1)-(2S,3R,4E)-2-N-tetracosanoylsphingenine, O--(2->3)-O-β-D-galactopyranosyl-(1->1)-(2S,3R,4E)-2-N-tetracosanoylsphingenine and O--(2->3)-O-α-D-galactopyranosyl-(1->1)-(2S,3R,4E)-2-N-tetracosanoylsphingenine by using O-3)-2,3,4,6-tetra-O-acetyl-D-galactopyranosyl trichloroacetimidate and O--(2->3)-2,4,6,tri-O-acetyl-D-galactopyranosyl trichloroacetimidate as key glycosyl donors, and (2S,3R,4E)-3-O-benzoyl-2-N-tetracosanoylsphingenine as a key glycosyl acceptor.

ENTWICKLUNG EINES SYNTHESEBLOCKS DER 3-O-β-D-GALACTOPYRANOSYL-D-GALACTOPYRANOSE

In the presence of trimethylsilyl triflate, 1,2,3,4,6-penta-O-acetyl-β-D-galactopyranose reacted with benzyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside to give benzyl 2,6-di-O-benzyl-3-O-β-D-galactopyranosyl-β-D-galactopyranoside further converted i

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

SYNTHESIS OF THE TETRASACCHARIDE REPEATING UNIT OF THE O-SPECIFIC POLYSACCHARIDE FROM SALMONELLA MUENSTER AND SALMONELLA MINEAPOLIS

The tetrasaccharide β-D-Man-(1-->4)-α-L-Rha-(1-->3)-D-Gal-(4--1)-α-D-Glc the repeating unit of the O-specific polysaccharide chain of the lipopolysaccharides from Salmonella muenster and S. mineapolis was obtained by glycosylation of benzyl 2,6-di-O-benz