491-85-0

Upstream product

• 1225015-63-3 C₂₁H₃₁NO₁₁ 
• 65372-00-1 2-methyl-(3-O-acetyl-4,6-di-O-benzyl-1,2-dideoxy-α-D-glucopyrano)-<2,1-d>-2-oxazoline 
• 61236-91-7 3-O-acetyl-2,4,6-tri-O-benzyl-D-galactopyranosyl bromide 
• 78139-09-0 benzyl 3-O-acetyl-2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 78139-07-8 3-O-acetyl-2,4,6-tri-O-benzyl-β-D-galactopyranosyl benzylxanthate 
• 78139-16-9 benzyl 3-O-(2-acetamido-4,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 78139-15-8 benzyl 3-O-(2-acetamido-3-O-acetyl-4,6-di-O-benzyl-2-deoxy-β-D-glucopyranosyl)-2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 78139-08-9 benzyl 2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 83032-25-1 3-O-(2-Acetamido-2-desoxy-6-O-trityl-α-D-galactopyranosyl)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 61865-88-1 3-O-(3,4-didesoxy-6-O-trityl-α-D-glycero-hex-3-enopyranosyl)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 83032-23-9 (2R,4R,5R,6R)-2-[(3aR,5R,6S,6aR)-5-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yloxy]-4,5-dihydroxy-6-trityloxymethyl-dihydro-pyran-3-one oxime 
• 79705-45-6 1,6-Di-O-acetyl-3-O-(6-O-acetyl-2-acetamido-3,4-di-O-benzyl-2-desoxy-α-D-glucopyranosyl)-2,4-di-O-benzyl-D-galactopyranose 
• 79705-47-8 Acetic acid (3R,4S,5S,6R)-6-acetoxymethyl-4-((2R,3R,4R,5S,6R)-6-acetoxymethyl-3-acetylamino-4,5-dihydroxy-tetrahydro-pyran-2-yloxy)-3,5-dihydroxy-tetrahydro-pyran-2-yl ester 
• 83032-25-1 3-O-(2-Acetamido-3,4-di-O-acetyl-2-desoxy-6-O-trityl-α-D-talopyranosyl)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 

Downstream Products

• 62397-85-7 N-{(2S,3R,4R,5S,6R)-2-[(1R,2S)-1-(1,2-Dihydroxy-ethyl)-2,3,4-trihydroxy-butoxy]-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl}-acetamide 

Relevant academic research and scientific papers

DISACCHARIDES

A disaccharide having the structure (Formula I), and a disaccharide having the structure (Formula II) exhibit immunomodulatory activity.

SYNTHESE DE DISACCHARIDES A LIAISON α-D PAR CYCLOADDITION: 3-O-α-L-FUCOPYRANOSYL-D-GLUCOSE, 3-O-(2-ACETAMIDO-2-DESOXY-α-D-GALACTOPYRANOSYL)-D-GLUCOSE ET 3-O-α-D-TALOPYRANOSYL-D-GLUCOSE

Reduction of the primary alcohol group of 1,2:5,6-isopropylidene-3-O-(2,3,4-trideoxy-α-L-glycero-hex-2-enopyranosyl)-α-D-glucofuranose by p-toluenesulfonylation, substitution by iodine, and tributylstannane treatment, gave a 6'-deoxy derivative, which was

Bausteine von Oligosacchariden, XXIX. Synthese des Trisaccharids aus N-Acetylglucosamin, Galactose und Rhamnose einer O-determinanten Kette von Escherichia coli. Abhaengigkeit der Stereoselektivitaet der α-Glycosidsynthese von der Reaktivitaet des Pyranos

The mercury salt catalysed reaction of substituted α-D-galactosyl halides with the reactive 4-OH groups of the rhamnosides 18 and 19 were studied.The order of reactivity of the halides increases with the following substituents: O-acetyl O-glucosyl O-b

PARTIALLY BENZYLATED OXAZOLINE DERIVATIVES OF 2-ACETAMIDO-2-DEOXY-D-GLUCOPYRANOSE AS "STANDARDIZED INTERMEDIATES" FOR OLIGOSACCHARIDE SYNTHESIS. PREPARATION OF DISACCHARIDES HAVING THE SEQUENCES β-D-GlcpNAc(1->x)-D-Gal AND β-D-GlcpNAc(1->4)-D-GlcNAc

Three benzyl tri-O-benzyl-1-thio-β-D-galactopyranosides (5, 6, and 7) were prepared from the corresponding O-acyltri-O-benzyl-D-galactopyranosyl bromides (1a-c) via the benzylxanthates 2a-c and the fully protected benzyl thiogalactosides 3a-c.The α anomer