213766-35-9

Upstream product

• 629-41-4 1,8-Octanediol 
• 38257-96-4 8-[(triphenylmethyl)oxy]octanol 
• 63167-69-1 methyl 2,3-O-isopropylidene-α-D-mannopyranoside 
• 213767-23-8 methyl 4-O-benzyl-2,3-O-isopropylidene-6-O-(8'-trityloxyoctyl)-α-D-mannopyranoside 
• 65686-45-5 Methanesulfonic acid 8-trityloxy-octyl ester 
• 213767-26-1 methyl 4-O-benzyl-6-O-(8'-hydroxyoctyl)-α-D-mannopyranoside 
• 150161-11-8 Methyl 4-O-benzyl-6-O-tert-butyldiphenylsilyl-2,3-di-O-isopropylidene-α-D-mannopyranoside 
• 131089-35-5 methyl 6-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-α-D-mannopyranoside 
• 82185-79-3 methyl 4-O-benzyl-2,3-O-isopropylidene-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 124-63-0 methanesulfonyl chloride 
• 213767-29-4 methyl 3-O-allyl-4-O-benzyl-6-O-(8'-hydroxyoctyl)-α-D-mannopyranoside 

Downstream Products

• 213768-39-9 (1S,3R,4R,5S,6S,7R,20R,22S,23S,24R)-4,5,6,24-Tetrakis-benzyloxy-23-((2R,3R,5R,6R)-3,5-bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-22-methoxy-2,9,18,21,25-pentaoxa-tricyclo[18.2.2.1^3,7]pentacosane 
• 213768-53-7 Methanesulfonic acid 8-[(2R,3R,4S,5S,6S)-4-allyloxy-3-benzyloxy-6-methoxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-ylmethoxy]-octyl ester 
• 213768-01-5 methyl 2-O-(3'-O-allyl-4'-O-benzyl-α-D-galactopyranosyl)-2,3,4-tri-O-benzyl-6,6'-di-O-(octane-1,8-diyl)-α-D-mannopyranoside 
• 213768-21-9 methyl 2-O-(2',3',4'-tri-O-benzyl-α-D-galactopyranosyl)-4-O-benzyl-6,6'-di-O-(octane-1,8-diyl)-α-D-mannopyranoside 
• 213768-46-8 Methanesulfonic acid 8-[(2R,3R,4S,5S,6S)-4-allyloxy-3-benzyloxy-6-methoxy-5-((2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-trityloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-ylmethoxy]-octyl ester 

Relevant academic research and scientific papers

Synthesis of Tethered Trisaccharides to Probe Inter-Saccharide Flexibility in Carbohydrate - Protein Interactions

Two crystal structures of the trisaccharide epitope α-D-Galp(1→2)[α-D-Abep(1→3)α-D-Manp1→OCH 3 1 bound to antibody Fab and single-chain Fv fragments have been used to guide the design of an intramolecular tether that constrains the trisaccharid