144431-90-3

Upstream product

• 90164-77-5 methyl [2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->3)]-4-O-benzyl-α-L-rhamnopyranoside 
• 14218-08-7 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl bromide 
• 161007-95-0 2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyltrichloroacetimidate 
• 78153-79-4 2,3,4,6-tetra-O-benzyl-D-glucopyranosyl fluoride 
• 247092-69-9 methyl (2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1->2)-4-O-benzyl-α-L-rhamnopyranoside 
• 71715-59-8 methyl 2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 4196-35-4 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl bromide 
• 247092-68-8 methyl (2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1->2)-3-O-allyl-4-O-benzyl-α-L-rhamnopyranoside 
• 69558-09-4 methyl 3-O-allyl-4-O-benzyl-α-L-rhamnopyranoside 
• 25019-69-6 methyl 4-O-benzyl-α-L-rhamnopyranoside 
• 67773-43-7 2,3,4,6-tetra-O-benzyl-α/β-D-glucopyranosyl bromide 

Downstream Products

• 247092-66-6 methyl (2,3,4-tri-O-benzoyl-α-L-rhamnopyranosyl)-(1->2)-[α-D-glucopyranosyl-(1->3)]-α-L-rhamnopyranoside 

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 and (13)C NMR spectra of 2,3-di-O-glycosyl derivatives of methyl α-L-rhamnopyranoside and methyl α-D-mannopyranoside

The syntheses are described of 2,3-di-O-glycosyl derivatives of methyl α-L-rhamnopyranoside (1-5) and α-D-mannopyranoside (6-9). The deviation from additivity in (13)C NMR spectra calculated for 1-9 were similar for stereochemically rela