125946-77-2

Upstream product

• 100-39-0 benzyl bromide 
• 125946-76-1 allyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 114853-29-1 allyl 2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 1093115-83-3 p-methylphenyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 129445-36-9 allyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 89067-86-7 allyl 3-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 136882-36-5 2-((2S,3R,4R,5S,6R)-4,5-Dihydroxy-6-hydroxymethyl-2-phenylsulfanyl-tetrahydro-pyran-3-yl)-isoindole-1,3-dione 
• 196697-91-3 phenyl 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 

Downstream Products

• 125946-65-8 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate 
• 134154-74-8 3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl chloride 
• 134136-29-1 8-(methoxycarbonyl)octyl 2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-4-O-benzyl-α-L-rhamnopyranoside 
• 134136-26-8 allyl 3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-4-O-benzyl-α-L-rhamnopyranoside 
• 134136-24-6 allyl 3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-2-O-acetyl-4-O-benzyl-α-L-rhamnopyranoside 
• 134136-27-9 8-(methoxycarbonyl)octyl 4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside 
• 134136-25-7 8-(methoxycarbonyl)octyl 2-O-benzoyl-4-O-benzyl-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-L-rhamnopyranoside 
• 134136-28-0 allyl 2-O-(2-O-acetyl-3,4-di-O-benzyl-α-L-rhamnopyranosyl)-3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-4-O-benzyl-α-L-rhamnopyranoside 

Relevant academic research and scientific papers

Synthesis of the Campylobacter jejuni 81-176 Strain Capsular Polysaccharide Repeating Unit Reveals the Absolute Configuration of its O-Methyl Phosphoramidate Motif

The O-methyl phosphoramidate (MeOPN) motif is a non-stoichiometric modification of capsular polysaccharides (CPS) in ≈70 % of all Campylobacter jejuni strains. Infections by C. jejuni lead to food-borne illnesses and the CPS they produce are key virulence

Ketone-imide versus ketone-oxime reductive cross-coupling promoted by samarium diiodide: New mechanistic insight gained from a failed aminocyclopentitol synthesis

The intramolecular 1,6-ketone/imide reductive coupling promoted by samarium diiodide competes favorably with an alternative 1,5-ketone/oxime ether coupling in a keto-oxime substrate derived from D-glucosamine N-protected with a phthalimido group. This pin

Synthesis and n.m.r. analysis of branched trisaccharide and pentasaccharide haptens of the β-hemolytic Streptococci Group A and the preparation of synthetic antigens

The synthesis of branched trisaccharide and pentasaccharide portions of the cell-wall polysaccharide of the β-hemolytic Streptococci Group A is described.The key disaccharide acceptors, allyl or 8-(methoxycarbonyl)octyl 3-O-(3,4,6-tri-O-benzyl-2-deoxy-2-p

Synthesis of an appropriately protected core glycotetraoside, a key intermediate for the synthesis of "bisected" complex-type glycans of a glycoprotein.

A stereocontrolled synthetic route to a glycotetraoside, allyl O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranosyl)-(1--- -4)-O- (3,6-di-O-allyl-2-O-benzyl-beta-D-mannopyranosyl)-(1----4)-O-3, 6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-gluco