112107-24-1

Upstream product

• 25019-69-6 methyl 4-O-benzyl-α-L-rhamnopyranoside 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 137493-19-7 C₇₅H₆₈O₂₁ 
• 137493-19-7 C₇₅H₆₈O₂₁ 
• 137493-20-0 Methyl 3-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-(2,3,4-tri-O-benzoyl-β-L-fucopyranosyl)-α-L-rhamnopyranoside 
• 137493-20-0 Methyl 3-O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-2-O-(2,3,4-tri-O-benzoyl-β-L-fucopyranosyl)-α-L-rhamnopyranoside 
• 137439-14-6 C₆₈H₆₄O₁₉ 
• 137439-15-7 Methyl 2-O-(2,3,4-tri-O-benzoyl-β-L-fucopyranosyl)-3-O-(2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-α-L-rhamnopyranoside 
• 137439-08-8 Methyl 4-O-benzyl-2-O-(2,3,4-tri-O-benzoyl-α-L-fucopyranosyl)-α-L-rhamnopyranoside 
• 137439-07-7 C₄₉H₅₀O₁₃ 
• 137439-13-5 1,3,4-tri-O-benzoyl-α-L-fucopyranose 

Relevant academic research and scientific papers

Synthesis of a tri- and tetrasaccharide fragment specific for the Shigella flexneri serotype 5a O-antigen. A reinvestigation

Stereocontrolled, stepwise synthesis of methyl α-L-rhamnopyranosyl-(1→2)-[α-D-glucopyranosyl-(1→3)]-α-L-rhamnopyranoside (A(E)B, 1) and methyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranosyl -(1→2)-[α-D-glucopyranosyl-(1 →3)]-α-L-rhamnopy

Synthesis of di-O-glycosyl derivatives of methyl α-L-rhamnopyranoside

The syntheses are described of 2,3-di-O-glycosyl derivatives (1-12) of methyl α-L-rhamnopyranoside where the glycosyl moieties are variously α-L-fucopyranose, β-L-fucopyranose, β-D-glucopyranose, α-D-mannopyranose, and α-L-rhamnopyranose.The syntheses inv