182167-81-3

Upstream product

• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 182167-71-1 Methyl 2,3-O-isopropylidene-4-O-(p-methoxybenzyl)-α-D-rhamnopyranoside 
• 182167-73-3 Methyl 4-O-(p-methoxybenzyl)-α-D-rhamnopyranoside 
• 182167-79-9 Benzoic acid (2S,3S,5S,6R)-5-hydroxy-2-methoxy-6-methyl-tetrahydro-pyran-3-yl ester 
• 112612-45-0 methyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 98-88-4 benzoyl chloride 
• 32476-35-0 Methyl 2,4-di-O-benzoyl-3,6-dideoxy-α-D-arabino-hexopyranoside 
• 182167-80-2 1-O-Acetyl 2,4-di-O-benzoyl-3,6-dideoxy-α-D-arabino-hexopyranose 
• 75-08-1 ethanethiol 
• 182167-77-7 Benzoic acid (2S,3S,5S,6R)-2-methoxy-5-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-3-yl ester 
• 182167-74-4 Methyl 4-O-(p-methoxybenzyl)-2,3-O-sulfonyl-α-D-rhamnopyranoside 
• 182167-72-2 Toluene-4-sulfonic acid (3aS,4S,6R,7R,7aS)-4-methoxy-7-(4-methoxy-benzyloxy)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethyl ester 

Downstream Products

• 182167-87-9 Allyl 2-O-benzoyl-3-O-(2,4-di-O-benzoyl-3,6-dideoxy-α-D-arabino-hexopyranosyl)-α-D-mannopyranoside 
• 182167-86-8 Allyl 2-O-benzoyl-3-O-[2,4-di-O-benzoyl-3,6-dideoxy-4-O-(p-methoxybenzyl)-α-D-arabino-hexopyranosyl]-4,6-di-O-(p-methoxybenzyl)-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of and molecular dynamics simulations on a tetrasaccharide corresponding to the repeating unit of the capsular polysaccharide from Salmonella enteritidis

Syntheses of two oligosaccharides as methyl glycosides related to the repeating unit of S. enteritidis capsular polysaccharide (CPS) are presented. The trisaccharide corresponds to the backbone of the CPS whereas the tetrasaccharide is a model for the rep

Preparation of disaccharide haptens corresponding to Salmonella serogroups B and D

The properly protected ethyl 1-thio-abequopyranoside 11 and ethyl 1-thio-tyvelo-pyranoside 26 were prepared by a sequence of reactions, the key step of which was the regioselective hydride-mediated ring-opening of the cyclic sulfate function in compounds 8 and 18. Iodonium ion-assisted glycosylation of allyl mannopyranoside 30 with the individual ethyl 3,6-dideoxy-1-thio-D-hexopyranoside donors 11 and 26 furnished, after deprotection, the respective allyl 3-O-(α-D-abequopyranosyl)-α-D-mannopyranoside 1 and allyl 3-O-(α-D-tyvelopyranosyl)-α-D-mannopyranoside 2.