115945-98-7

Upstream product

• 76419-48-2 methyl 4,6-O-benzylidene-3-O-benzyl-α-D-glucopyranoside 
• 94160-77-7 methyl 2-O-trifluoromethanesulfonyl-3-O-benzyl-(R)-4,6-O-benzylidene-α-D-glucopyranoside 
• 108-24-7 acetic anhydride 
• 94160-78-8 methyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-mannopyranoside 
• 116003-78-2 Methyl 2-azido-2-deoxy-4,6-O-(phenylmethylene)-α-D-mannopyranoside 
• 115945-96-5 methyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(N-imidazolylsulfonyl)-α-D-altropyranoside 
• 115945-97-6 methyl 3-O-acetyl-2-azido-4,6-O-benzylidene-2-deoxy-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 116003-77-1 2-azido-2-deoxy-4,6-O-(phenylmethylene)methyl-α-D-altropyranoside 
• 94119-09-2 methyl 2-azido-3-O-benzyl-2-deoxy-α-D-mannopyranoside 

Downstream Products

• 115946-00-4 2,2,2-trichloroethyl 2-O-<2,3-tri-O-benzyl-4-O-(4,6-di-O-acetyl-2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-α-D-glucopyranosyl>-3,4-di-O-benzyl-α-L-rhamnopyranoside 
• 115946-05-9 8-(methoxycarbonyl)octyl 2-O-<2-acetamido-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-β-D-mannopyranosyl-2,3,6-tri-O-benzyl-α-D-glucopyranosyl>-3,4-di-O-benzyl-β-L-rhamnopyranoside 
• 115946-06-0 8-(methoxycarbonyl)octyl 2-O-<4-O-(2-acetamido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranosyl>-3,4-di-O-benzyl-β-L-rhamnopyranoside 
• 115946-02-6 2-O-<4-O-(2-acetamido-4,6-di-O-acetyl-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranosyl>-3,4-di-O-benzyl-α,β-L-rhamnopyranose 
• 115946-03-7 2-O-<4-O-(2-acetamido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranosyl>-3,4-di-O-benzyl-α,β-L-rhamnopyranose 
• 115945-99-8 4,6-di-O-acetyl-2-azido-3-O-benzyl-2-deoxy-α-D-mannopyranosyl bromide 

Relevant academic research and scientific papers

Mannosazide methyl uronate donors. Glycosylating properties and use in the construction of β-ManNAcA-containing oligosaccharides

Mannosazide methyl uronate donors equipped with a variety of anomeric leaving groups (β- and α-S-phenyl, β- and α-N- phenyltrifluoroacetimidates, hydroxyl, β-sulfoxide, and (Rs)- and (Ss)-α-sulfoxides) were subjected to activating co

SYNTHESIS OF A TRISACCHARIDE COMPONENT OF THE CAPSULAR POLYSACCHARIDE OF Streptococcus pneumoniae TYPE 19F

2-O--α,β-L-rhamnopyranose, a structural component of the capsular polysaccharide of Streptococcus pneumoniae type 19F, has been synthesized by sequential glycosylation reactions using the gl