134221-38-8

Upstream product

• 763129-77-7 phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-α-D-glucopyranoside 
• 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 

Downstream Products

• 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 
• 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 
• 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 
• 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 

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

Modification of Cyclodextrins by Insertion of a Heterogeneous Sugar Unit into Their Skeletons. Synthesis of 2-Amino-2-deoxy-β-cyclodextrin from α-Cyclodextrin

Acetolysis of fully acetylated α-cyclodextrin 5a resulted in restricted fission of only one of the glycosidic bond to give the acyclic maltohexaose peracetate 6a in 46percent yields.Regioselective modifications of both terminals of hexasaccharide 6a were