183954-75-8

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 48149-72-0 (2S,3R,4S,5R,6R)-2-Allyloxy-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

Downstream Products

• 183954-76-9 allyl 2,4,6-tri-O-benzyl-3-O-(4-methoxybenzyl)-α-D-galactopyranoside 
• 61236-87-1 allyl 2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 169836-51-5 allyl 3-O-<2-acetamido-2-deoxy-3-O-(3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-β-D-galactopyranosyl>-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 169836-50-4 allyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl-(1->3)-2-acetamido-2-deoxy-4,6-di-O-pivaloyl-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 402578-72-7 allyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 402578-68-1 allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 402578-76-1 allyl 2-acetamido-2-deoxy-3,6-di-O-pivaloyl-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 402578-80-7 allyl 2-acetamido-2-deoxy-4,6-di-O-pivaloyl-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 402578-89-6 allyl 3,4,6-tri-O-benzyl-β-D-galactopyranosyl-(1->3)-2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 171411-34-0 ((2S,3R,4S,5S,6R)-2-Allyloxy-3,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yloxy)-trimethyl-silane 

Relevant academic research and scientific papers

Improvement of the synthesis of immunological carbohydrate vaccines containing the tumour associate antigen CaMBr1

The simplified synthesis of a portion of Globo-H hexasaccharide, a saccharide antigen overexpressed by breast cancer cells, and its conjugation to two different immunogenic proteins are described. The conjugated vaccines, evaluated in a preclinical model, showed good immunogenic potential.

Rational design and synthesis of a 1,1-linked disaccharide that is 5 times as active as sialyl Lewis X in binding to E-selectin

We describe here a rational design and synthesis of (3-O-carboxymethyl)-β-D-galactopyranosyl α-D-mannopyranoside which is 5 times as active as sialyl Lewis X in binding to E-selectin and also effective against P- and L-selectin. A new method for the 1,1-g