19474-56-7

Upstream product

• 100-39-0 benzyl bromide 
• 92733-57-8 methyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 92733-58-9 methyl 2,6-di-O-benzyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 914772-34-2 methyl 2,3,6,2',3'-penta-O-benzyl-4',6'-O-benzylidene-β-lactoside 
• 30021-61-5 methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 
• 7216-69-5 methyl β-D-lactopyranoside 
• 4753-07-5 α-hepta-O-acetylmaltosyl bromide 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 98151-13-4 methyl 2,3,6-tri-O-benzyl-4-O-(2,6-di-O-benzyl-3,4-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 92733-55-6 methyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-cyclohexylidene-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 92733-56-7 methyl 2,3,6-tri-O-benzyl-4-O-(2,6-di-O-benzyl-3,4-O-cyclohexylidene-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 92733-59-0 methyl 4-O-(6-O-acetyl-2,3-di-O-benzyl-β-D-galactopyranosyl)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 1426575-72-5 C₆₀H₆₀O₁₀S 
• 98151-12-3 methyl 2,3,6-tri-O-benzyl-4-O-(2,6-di-O-benzyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-β-D-glucopyranoside 

Downstream Products

• 92733-72-7 methyl O-(4-O-acetyl-3,6-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-β-D-glucopyranoside) 
• 914772-40-0 acetic acid 3-acetoxy-2-acetoxymethyl-6-[4,5-bis-benzyloxy-2-benzyloxymethyl-6-(4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yloxy]-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-4-yl ester 
• 1357376-97-6 methyl 2,3,6-tri-O-benzyl-4-O-(2',3',6'-tri-O-benzyl-4'-O-(4''-chlorobutyl)-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 1357376-98-7 methyl 2,3,6-tri-O-benzyl-4-O-(2',3',6'-tri-O-benzyl-4'-O-(4''-iodobutyl)-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 1357376-99-8 methyl 2,3,6-tri-O-benzyl-4-O-(2',3',6'-tri-O-benzyl-4'-O-(5'',5''-di-tert-butoxycarbonylpentyl)-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 1426575-86-1 C₈₃H₈₈O₁₇ 
• 1426575-87-2 C₈₃H₈₈O₁₇ 
• 1426576-19-3 C₈₃H₈₈O₁₇ 
• 1426576-25-1 C₈₃H₈₈O₁₇ 
• 116235-03-1 methyl 2,3,6-tri-O-benzyl-4-O-(2,3,6-tri-O-benzyl-4-deoxy-β-D-xylo-hexopyranosyl)-β-D-glucopyranoside 
• 92733-71-6 methyl O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-benzyl-β-D-glucopyranoside) 
• 98151-14-5 Acetic acid (2R,3S,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-((2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Reagent Controlled Stereoselective Synthesis of α-Glucans

The development of a general glycosylation method that allows for the stereoselective construction of glycosidic linkages is a tremendous challenge. Because of the differences in steric and electronic properties of the building blocks used, the outcome of

Synthesis of a series of maltotriose phosphates with an evaluation of the utility of a fluorous phosphate protecting group

A series of methyl maltotrioside phosphates were synthesized for application in the determination of the actual molecular substrate of the Lafora enzyme involved in Lafora disease. Several different synthetic routes were applied for the successful synthesis of six methyl maltotrioside phosphate regioisomers. The utility of a new fluorous phosphate protecting group was also evaluated, but its utility was found to be limited in this particular late stage introduction.

An efficient glycosylation reaction for the synthesis of asialo GM2 analogues

We investigated the coupling reaction of glycosyl donors N-trichloroethoxycarbonyl-galactosamine-O-trichloroacetimidate (2a) and N-p-nitrobenzyloxycarbonyl-galactosamine-O-trichloroacetimidate (2b) with the 4′-OH of lactose derivatives (3a-d) to synthesiz

Studies of the molecular recognition of synthetic methyl β-lactoside analogues by Ricinus communis agglutinin

The 2-, 3-, 6-, 2'-, 3'-, 4'-, and 6'-deoxy derivatives and the 3-O-methyl derivative of methyl β-lactoside have been synthesised and their binding to the galactose-specific agglutinin from Ricinus communis (RCA-120) has been investigated. The results ind

SYNTHESIS OF DI-, TRI-, AND TETRA-SACCHARIDES CORRESPONDING TO RECEPTOR STRUCTURES RECOGNISED BY Streptococcus pneumoniae

Syntheses are described for methyl 2-acetamido-2-deoxy-4-O-β-D-galactopyranosyl-α-D-glucopyranoside, methyl 2-acetamido-2-deoxy-4-O-β-D-galactopyranosyl-β-D-glucopyranoside, methyl 3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-β-D-galactopyranoside, methyl

SYNTHESIS OF THE TRISACCHARIDE MOIETY OF GANGLIOTRIOSYLCERAMIDE (ASIALO GM2)

The synthesis of the trisaccharide methyl glycoside β-D-GalNAc-(1->4)-β-D-Gal-(1->4)-β-D-Glc-OMe, which corresponds to the carbohydrate portion of gangliotriosylceramide (asialo GM2), was accomplished by the reaction of 4-O-acetyl-3,6-di-O-benz