62098-37-7

Upstream product

• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 1281971-23-0 benzyl 3,4,6-tri-O-benzyl-2-[(tert-butoxycarbonyl)amino]-2-deoxy-D-glucopyranoside 
• 3068-36-8 3,4,6-tri-O-acetyl-2-deoxy-2-(2,4-dinitroanilino)-α-D-glucopyranosyl bromide 
• 7784-55-6 Tetraacetyl-<2,4-dinitrophenyl>-glucosamin 
• 111240-23-4 benzyl 2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside 
• 262599-29-1 benzyl 3,4,6-tri-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D-glucopyranoside 

Downstream Products

• 1415608-17-1 (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-phenyltetrahydro-2H-pyran-3-amine 
• 121409-03-8 (2R,3R,4R,5S,6R)-6-(hydroxymethyl)-3-(phenylamino)tetrahydro-2H-pyran-2,4,5-triol 
• 1415608-19-3 (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-p-tolyltetrahydro-2H-pyran-3-amine 
• 1415608-21-7 (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(4-methoxyphenyl)tetrahydro-2H-pyran-3-amine 
• 1415608-23-9 (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(4-chlorophenyl)tetrahydro-2H-pyran-3-amine 
• 1415608-25-1 (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(4-bromophenyl)tetrahydro-2H-pyran-3-amine 
• 1415608-28-4 ethyl 4-((2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)tetrahydro-2H-pyran-3-ylamino)benzoate 
• 1476029-39-6 (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(o-tolyl)tetrahydro-2H-pyran-3-amine 
• 1476029-40-9 (2R,3R,4R,5S,6R)-2,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-N-(2-methoxyphenyl)tetrahydro-2H-pyran-3-amine 
• 1423122-16-0 benzyl 3,4,6-Tri-O-benzyl-2-deoxy-2-(L-prolylamino)-β-D-glucopyranoside 
• 4171-69-1 Benzyl 2-N-acetylamino-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside 

Relevant academic research and scientific papers

Stereoselective Synthesis of 1,1′-Disaccharides by Organoboron Catalysis

The highly stereoselective synthesis of 1,1′-disaccharides was achieved by using 1,2-dihydroxyglycosyl acceptors and glycosyl donors in the presence of a tricyclic borinic acid catalyst. In this reaction, the complexation of the diols and the catalyst is

Synthesis and characterization of monosaccharide derivatives and application of sugar-based prolinamides in asymmetric synthesis

For the first time, the β-anomer of N-acetylglucosamine derivative methyl 2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside (9b) was synthesized, isolated, and used in the synthesis of sugar-based primary amine 4b. Sugar-based primary amine 5a, a

Glucosamine-based primary amines as organocatalysts for the asymmetric aldol reaction

Glucosamine derivatives have been synthesized starting from commercially available N-acetyl-D-glucosamine/glucosamine hydrochloride and have been employed successfully as efficient organocatalysts for the direct asymmetric aldol reaction between cyclohexa

Benzyl derivatives of N-2,4-dinitrophenyl-D-glucosamine and their use for oligosaccharide synthesis

Four tri-O-benzyl derivatives of 2-deoxy-2-(2,4-dinitroanilino)-D- glucopyranose were synthesized. Glycosylation using 3,4,6-tri-O-benzyl-2- deoxy-2-(2,4-dinitroanilino)-D-glucopyranose as glycosyl donor and a reagent mixture of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, and triethylamine produced β-glycosides with complete selectivity. Starting from benzyl 3,6-di-O-benzyl-2-deoxy-2-(2,4-dinitroanilino)-β-D- glucopyranoside as acceptor, O-α-D-galactopyranosyl-(1 → 4)-O-β-D- galactopyranosyl-(1 → 4)-2-acetamido-2-deoxy-D-glucopyranose, the human blood-group P1-antigenic determinant, was synthesized.