889129-00-4

Upstream product

• 123-76-2 levulinic acid 
• 141810-60-8 ethyl 3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 20701-61-5 ethyl 4,6-O-benzylidene-1-thio-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 904689-93-6 p-methoxyphenyl 3-O-benzyl-4,6-O-benzylidene-2-O-levulinoyl-β-D-glucopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 1198156-19-2 dimethylthexylsilyl O-(2-O-levulinoyl-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyl)-(1->4)-O-2-azido-3-O-benzyl-6-O-levulinoyl-2-deoxy-β-D-glucopyranoside 
• 1198156-89-6 N-(benzyl)-benzyloxycarbonyl-5-aminopentyl O-(2-O-levulinoyl-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyl)-(1->4)-O-2-azido-3-O-benzyl-6-O-acetyl-2-deoxy-α-Dglucopyranoside 
• 1198156-91-0 N-(benzyl)-benzyloxycarbonyl-5-aminopentyl O-(2-O-levulinoyl-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyl)-(1->4)-O-2-azido-3-O-benzyl-6-O-levulinoyl-2-deoxy-α-D-glucopyranoside 
• 1198156-16-9 dimethylthexylsilyl O-(2-levulinoyl-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyl)-(1->4)-O-2-azido-3-O-benzyl-6-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 889129-06-0 3β-O-{(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->2)-[(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-(1->3)]-4,6-O-benzylidene-β-D-glucopyranosyl}cholesterol 
• 889129-04-8 3β-O-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->2)-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranosyl]cholesterol 
• 889129-05-9 3β-O-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->2)-4,6-O-benzylidene-β-D-glucopyranosyl]cholesterol 

Relevant academic research and scientific papers

HEPARAN SULFATE SYNTHESIS

The invention provides an efficient modular chemical synthesis for heparan sulfate oligosaccharides based on orthogonal protection strategies. Modular disaccharide building blocks, themselves the product of a novel combinatorial synthesis, are combined in

Modular synthesis of heparan sulfate oligosaccharides for structure-activity relationship studies

Although hundreds of heparan sulfate binding proteins have been identified and implicated in a myriad of physiological and pathological processes, very little information is known about the ligand requirements for binding and mediating biological activiti

Synthesis of saponins with cholestanol, cholesterol, and friedelanol as aglycones

Procedures for the synthesis of branched Xylss(1→3)[Galss- (1→2)]-Glc and Xylss(1→3)[Galss(1→2)]-GlcUA trisaccharides ss-linked to the 3-O of cholesterol, cholestanol, and friedelanol, respectively, were developed. To this end, ss-selective glucosylation

Synthesis of N-glycan oxazolines: donors for endohexosaminidase catalysed glycosylation

Oxazoline mono-, di-, tri- and hexasaccharides, corresponding to the core components of N-linked glycoprotein high mannose glycans, are synthesised as potential glycosyl donors for endohexosaminidase catalysed glycosylation of glycopeptides and glycoprote