313342-35-7

Upstream product

• 169393-72-0 2,3,4-tri-O-acetyl-6-O-benzyl-α,β-D-galactopyranosyl trichloroacetimidate 
• 481052-23-7 methyl O-(3,4-di-O-acetyl-2-O-benyzl-α-L-fucopyranosyl)-(1->3)-2-acetamido-2-deoxy-6-O-(2,2,2-trichloroethoxycarbonyl)-α-D-glucopyranoside 
• 481052-22-6 methyl O-(3,4-di-O-acetyl-2-O-benyzl-α-L-fucopyranosyl)-(1->3)-2-acetamido-2-deoxy-α-D-glucopyranoside 
• 6619-02-9 methyl N-acetyl-2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 

Downstream Products

• 313342-36-8 methyl O-(2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-[(3,4-di-O-acetyl-2-O-benzyl-α-L-fucopyranosyl)-(1->3)]-2-acetamido-2-deoxy-6-O-methylthiomethyl-α-D-glucopyranoside 
• 176106-81-3 methyl O-(β-D-galactopyranosyl)-(1->4)-[(α-L-fucopyranosyl)-(1->3)]-2-acetamido-2-deoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Carbohydrate-carbohydrate recognition between Lewis X blood group antigens, mediated by calcium ions

Bivalent Lewis X (LeX) oligosaccharides were synthesised in order to study the conformational details of carbohydrate clusters by NMR spectroscopy. To this end, two Lex trisaccharide moieties (1) were covalently linked through the 6-hydroxy group or through the anomeric oxygen of GlcNAc to yield dimers 2 and 3, respectively. The two Lex halves of the model saccharide 2 exhibited cooperativity in calcium binding. Three different lactosides served as control compounds for NMR titration with calcium chloride. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.