258286-43-0

Upstream product

• 75-36-5 acetyl chloride 
• 258286-29-2 methyl 2-azido-6-O-benzyl-2-desoxy-α-D-galactopyranoside 
• 68733-27-7 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranosyl iodide 
• 128716-56-3 2-azido-6-O-benzyl-2-deoxy-3,4-O-isopropylidene-β-D-galactopyranosyl nitrate 
• 258286-28-1 methyl 2-azido-6-O-benzyl-2-desoxy-3,4-O-isopropylidene-α-D-galactopyranoside 
• 670249-21-5 methyl 2-azido-4,6-O-benzylidene-2-deoxy-α-D-galactopyranoside 
• 670249-18-0 methyl 2-azido-2-deoxy-α/β-D-galactopyranoside 
• 67673-39-6 3,4,6-tri-O-acetyl-2-azido-2-deoxy-alpha-D-galactopyranosyl bromide 
• 894352-68-2 Acetic acid (2S,4aR,6S,7R,8R,8aR)-7-azido-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester 

Downstream Products

• 258286-60-1 methyl O-(2-azido-6-O-benzyl-2-desoxy-3,4-O-isopropylidene-α-D-galactopyranosyl)-(1->4)-O-(3-O-acetyl-2-azido-6-O-benzyl-2-desoxy-α-D-galactopyranosyl)-(1->4)-3-O-acetyl-2-azido-6-O-benzyl-2-desoxy-α-D-galactopyranoside 
• 893443-59-9 Benzoic acid (2R,3R,4S,5R,6R)-6-((2R,3R,4R,5R,6S)-4-acetoxy-5-azido-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yloxy)-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 893443-61-3 Benzoic acid (2R,3R,4S,5R,6R)-6-((2R,3R,4R,5R,6S)-5-azido-2-benzyloxymethyl-4-hydroxy-6-methoxy-tetrahydro-pyran-3-yloxy)-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 893443-60-2 (2S,3R,4R,5R,6R)-3-Azido-6-benzyloxymethyl-2-methoxy-5-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-ol 

Relevant academic research and scientific papers

Synthesis of a common trisaccharide fragment of glycoforms of the outer core region of the Pseudomonas aeruginosa lipopolysaccharide

The first synthesis of the common trisaccharide of glycoforms of the outer core region of the Pseudomonas aeruginosa lipopolysaccharide is reported. A fully protected trisaccharide precursor was prepared via a highly efficient α-(1→4)-glucosylation of a β

Synthesis of capsular polysaccharide oligomers of Salmonella typhi, bacteria originated from typhoid fever

The highly antigenic capsular polysaccharide of Salmonella typhi is a polysaccharide made out of N-acetyl D-galactosaminuronic acid units connected together through an α(1→4) linkage. Most of the hydroxyl groups at C-3 are acetylated. In order to determine the minimal size of fragments required for eliciting a significant immunological response, the corresponding di, tri, tetra and hexasaccharides have been chemically synthesized. The strategy is based on the use of anomeric S-xanthates of 2-azido-2-deoxy-D- galactopyranosyl derivatives as glycosyl donors. It has been shown that tetra and hexasaccharides are able to inhibit antibody binding by native polysaccharide.