763129-77-7

Upstream product

• 183875-35-6 phenyl 3,4,6-tri-O-acetyl-2-deoxy-2-azido-1-thiol-α-D-glucopyranoside 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 183875-22-1 phenyl 2-azido-2-deoxy-3,4,6-tri-O-acetyl-1-thio-α/β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 819870-57-0 phenyl 2-azido-3-O-benzyl-2-deoxy-4,6-O-p-methoxybenzylidene-1-thio-α-D-glucopyranoside 

Downstream Products

• 134221-38-8 6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-(p-methoxybenzyl)-D-glucopyranosyl trichloroacetamidate 
• 1394857-43-2 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-O-trichloroacetimidate-α-D-glucopyranoside 
• 1394857-61-4 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-O-trichloroacetimidate-β-D-glucopyranoside 
• 1394857-44-3 6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-α-D-glucopyranosyl-(1-4)-1,2-di-O-acetyl-3-O-benzyl-β-L-idopyranuronamide 
• 1394857-46-5 6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-α-D-glucopyranosyl-(1-4)-methyl 1,2-di-O-acetyl-3-O-benzyl-β-L-idopyranuronate 
• 1394857-49-8 methyl (phenyl 4-O-(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-α-D-glucopyranosyl)-2-O-acetyl-3-O-benzyl-1-thio-α-L-idopyranoside)-uronate 
• 1394857-56-7 methyl (phenyl 4-O-(6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-α-D-glucopyranosyl)-2-O-benzoyl-3-O-benzyl-1-thio-β-L-idopyranoside)-uronate 
• 915154-75-5 6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-α-D-glucopyranosyl-(1-4)-methyl-2-O-acetyl-3-O-benzyl-1-O-trichloroacetimidate-α/β-L-idopyranuronate 
• 1394857-58-9 6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-glucopyranosyl-(1-4)-methyl-1,2-di-O-acetyl-3-O-benzyl-β-L-idopyranuronate 
• 763129-73-3 phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-6-O-trifluoroethylsulfonate-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis and scalable conversion of L-iduronamides to heparin-related Di- and tetrasaccharides

A diastereomerically pure cyanohydrin, preparable on kilogram scale, is efficiently converted in one step into a novel L-iduronamide. A new regioselective acylation of this iduronamide and a new mild amide hydrolysis method mediated by amyl nitrite enable

Trifluoroethylsulfonate protected monosaccharides in glycosylation reactions

A variety of sulfo-protected monosaccharide donors and acceptors were investigated in glycosylation reactions. Trifluoroethylsulfonate (SO 3TFE) group was compatible with a wide range of activation conditions commonly used with fluoride, imidat