81713-25-9

Upstream product

• 81713-17-9 1-propenyl 2,3-di-O-benzoyl-4,6-di-O-benzyl-α-D-galactopyranoside 
• 81713-13-5 allyl 4,6-O-benzylidene-2,3-di-O-(2-butenyl)-α-D-galactopyranoside 
• 81713-16-8 1-propenyl 4,6-di-O-benzyl-α-D-galactopyranoside 
• 81713-14-6 (2R,3S,4S,5R,6S)-6-Allyloxy-4,5-bis-[((E)-but-2-enyl)oxy]-2-hydroxymethyl-tetrahydro-pyran-3-ol 
• 98-88-4 benzoyl chloride 
• 20746-64-9 allyl 4,6-O-benzylidene-α-D-galactopyranoside 
• 213020-57-6 methyl 2,3-di-O-benzoyl-6-O-benzyl-4-(4-bromobenzenesufonyl)-1-thio-β-D-glucopyranoside 
• 213020-60-1 methyl 2,3,6-di-O-benzyl-4-O-levulinoyl-1-thio-β-D-galactopyranoside 
• 213020-56-5 methyl 2,3-di-O-benzoyl-6-O-benzyl-1-thio-β-D-glucopyranoside 
• 148905-71-9 methyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 81713-21-5 2,3-di-O-benzoyl-4,6-di-O-benzyl-α,β-D-galactopyranose 

Downstream Products

• 88862-56-0 allyl O-(2,3-di-O-benzoyl-4,6-di-O-benzyl-β-D-galactopyranosyl)-(1<*>3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 106375-17-1 allyl O-(2,3-di-O-benzoyl-4,6-di-O-benzyl-β-D-galactopyranosyl)-(1<*>3)-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-(<1*>3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 106238-79-3 allyl O-(2,3-di-O-benzoyl-4,6-di-O-benzyl-β-D-galactopyranosyl)-(1<*>3)-O-(2-O-benzoyl-4,6-di-O-benzyl-β-D-galactopyranosyl)-(<1*>3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 584-30-5 3-O-β-galactopyranosyl-D-galactose 
• 88862-57-1 allyl O-(4,6-di-O-benzyl-β-D-galactopyranosyl)-(1<*>3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 106238-82-8 O-(2,3-di-O-benzoyl-4,6-di-O-benzyl-β-D-galactopyranosyl)-(1<*>3)-2-O-benzoyl-4,6-di-O-benzyl-α-D-galactopyranose 
• 106238-80-6 O-(2,3-di-O-benzoyl-4,6-di-O-benzyl-β-D-galactopyranosyl)-(1<*>3)-2-O-benzoyl-4,6-di-O-benzyl-α-D-galactopyranosyl chloride 
• 499-16-1 O-β-D-galactopyranosyl-(1->3)-D-galactitol 

Relevant academic research and scientific papers

Chemical synthesis of 13C-labelled ganglioside Gb3 trisaccharide from [U-13C]-D-glucose

The interaction of bacterial toxins with their cell surface glycolipid receptors offers scope for therapeutic intervention. Whilst crystal and solution structures of Escherichia coli verotoxin-1 have been reported, the precise nature of the interaction of

"STANDARDIZED INTERMEDIATES" FOR OLIGOSACCHARIDE SYNTHESIS. PRECURSORS OF D-GALACTOPYRANOSE RESIDUES HAVING CHAIN EXTENSION AT POSITION 3, OR POSITIONS 3 AND 2

A series of 2-O-benzoyl-4,6-di-O-benzyl-α-D-galactopyranosyl halides carrying either a second benzoyl group (8a, 12a) or a selectively removable, temporary protecting group (8b-d, 12b) at position 3 was synthesized from allyl α-D-galactopyranoside (1).The