134524-12-2

Upstream product

• 125519-98-4 methyl 3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 108-24-7 acetic anhydride 
• 148431-61-2 methyl 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 109526-95-6 methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 112612-45-0 methyl 2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 86447-92-9 methyl 4-O-benzyl-6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 100-44-7 benzyl chloride 

Downstream Products

• 128262-40-8 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranosyl chloride 
• 134407-34-4 ethyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-β-D-rhamnopyranoside 
• 134407-32-2 ethyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-α-D-rhamnopyranoside 
• 134407-43-5 methyl 2-O-(3,4-di-O-benzyl-α-D-rhamnopyranosyl)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 134407-42-4 methyl 2-O-(2-O-acetyl-3,4-di-O-benzyl-α-D-rhamnopyranosyl)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 134407-45-7 methyl O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(3,4-di-O-benzyl-α-D-rhamnopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 134407-40-2 methyl O-(3,4-di-O-benzyl-α-D-rhamnopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 134407-44-6 methyl O-(2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(3,4-di-O-benzyl-α-D-rhamnopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 134407-35-5 ethyl 2-O-(2-O-acetyl-3,4-di-O-benzyl-α-D-rhamnopyranosyl)-4-azido-3-O-benzyl-4,6-dideoxy-1-thio-α-D-mannopyranoside 
• 134407-39-9 methyl O-(2-O-acetyl-3,4-di-O-benzyl-α-D-rhamnopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 148431-62-3 1,2-anhydro-3,4-di-O-benzyl-6-deoxy-β-D-mannopyranose 
• 125519-98-4 methyl 3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 152174-34-0 ethyl 2-O-(3'-O-acetyl-2',4'-di-O-benzyl-α-D-rhamnopyranosyl)-3,4-di-O-benzyl-1-thio-α-D-rhamnopyranoside 
• 152174-29-3 ethyl 3,4-di-O-benzyl-2-O-(2',4'-di-O-benzyl-α-D-rhamnopyranosyl)-1-thio-α-D-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of a Trisaccharide Repeating Unit of the O-Antigen from Burkholderia multivorans and Its Oligomers

Burkholderia multivorans is a Gram-negative bacterium, and an important opportunistic human pathogen that can cause fatal infections. Its O-antigens are useful templates for the development of carbohydrate-based vaccines. A highly convergent and efficient

Synthesis of O-α-D-Rhap-(1 → 3)-O-α-D-Rhap-(1 → 2)-O-α-D-Rhap-(1 → 12)-oxydodecanoyl-bovine serum albumin

The title compound (19), a conjugate of a trisaccharide based upon the repeating trisaccharide of α-D-rhamnose, which comprises the polysaccharide portion of 'A-band' lipopolysaccharide from a mutant (AK1401) of Pseudomonas aeruginosa, strain PAO1, with b

Synthesis, conformational analysis, and the glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-β-L- and β-D-rhamnopyranoses

1,2-Anhydro-3,4-di-O-benzyl-α-L-rhamnopyranose was synthesized from L-rhamnose, while the D-enantiomer was synthesized from methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside. For both of the syntheses, the key intermediates were 2-O-acetyl-3,4-di-O-