85451-23-6

Upstream product

• 98-88-4 benzoyl chloride 
• 85451-17-8 1,2,3-tri-O-benzoyl-α-L-rhamnopyranose 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-L-rhamnoside 
• 178318-67-7 methyl 2,3-di-O-benzoyl-4-O-chloroacetyl-α-L-rhamnopyranoside 
• 178318-65-5 Chloro-acetic acid (3aR,4R,6S,7S,7aR)-4-methoxy-2,2,6-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester 
• 178318-66-6 methyl 4-O-chloroacetyl-α-L-rhamnopyranoside 
• 178318-68-8 1-O-acetyl-2,3-di-O-benzoyl-4-O-chloroacetyl-α-L-rhamnopyranoside 
• 85458-69-1 1,2,3-tri-O-benzoyl-4-O-chloroacetyl-α-L-rhamnopyranose 

Downstream Products

• 178318-73-5 (2R,3aS,5R,6R,7S,7aS)-7-Benzoyloxy-5-benzoyloxymethyl-6-[(2S,3R,4R,5S,6S)-3,4-bis-benzoyloxy-5-(2-chloro-acetoxy)-6-methyl-tetrahydro-pyran-2-yloxy]-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-2-carboxylic acid methyl ester 
• 90662-34-3 8-ethoxycarbonyloct-1-yl 2,3-di-O-benzoyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-α-L-rhamnopyranoside 
• 90662-32-1 8-ethoxycarbonyloct-1-yl 2,3-di-O-benzoyl-α-L-rhamnopyranoside 
• 178318-74-6 (2R,3aS,5R,6R,7S,7aS)-7-Benzoyloxy-5-benzoyloxymethyl-6-((2S,3R,4R,5S,6S)-3,4-bis-benzoyloxy-6-methyl-5-trityloxy-tetrahydro-pyran-2-yloxy)-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-2-carboxylic acid methyl ester 
• 178318-59-7 1,2-O-[1-(exo-cyano)ethylidene]-3,6-di-O-benzoyl-4-O-(2,3-di-O-benzoyl-4-O-trityl-α-L-rhamnopyranosyl)-α-D-mannopyranose 
• 178318-71-3 (2R,3aS,5R,6R,7S,7aS)-7-Benzoyloxy-5-benzoyloxymethyl-6-((2S,3R,4R,5S,6S)-3,4-bis-benzoyloxy-5-hydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-2-carboxylic acid methyl ester 
• 90662-31-0 C₃₃H₄₁ClO₁₀ 

Relevant academic research and scientific papers

Synthetic Cyclic Oligosaccharides - Syntheses and Structural Properties of a Cyclo(1->4)-α-L-rhamnopyranosyl-(1->4)-α-D-mannopyranosyl>trioside and -tetraoside

An efficient polycondensation-cyclization approach to the synthesis of cyclodextrin analogues is demonstrated by the preparation of cyclohexaoside 1 and cyclooctaoside 2.The key intermediate, disaccharide 3, bearing the cyanoethylidene group as a glycosyl

Mercury iodide as a catalyst in oligosaccharide synthesis.

The disaccharide 4-O-alpha-D-mannopyranosyl-alpha-L-rhamnopyranose and the trisaccharide 2-O-alpha-D-galactopyranosyl-4-O-beta-D-mannopyranosyl-alpha-L-rhamno pyranose determinants, which are analogs of the repeating unit of Salmonella sero-group A, B and

Syntheses of the Biological Repeating Units of Salmanella Serogroups A, B, and D1 O-Antigenic Polysaccharides

The immunogenic polysaccharide part of the Salmonella lipopolysaccharide of the cell walls of Salmonella bacteria belonging to serogroups A, B, and D1 is depicted below. Synthesis of the following three tetrasaccharides are described