174149-22-5

Upstream product

• 545-06-2 trichloroacetonitrile 
• 174149-28-1 2-(trimethylsilyl)ethyl 2,3-di-O-benzoyl-4-C-<(benzoyloxy)methyl>-6-O-benzyl-β-D-galactopyranoside 
• 174149-25-8 2-(trimethylsilyl)ethyl 2,3-di-O-benzoyl-6-O-benzyl-β-D-xylo-hexopyranosid-4-ulose 
• 174149-26-9 2-(trimethylsilyl)ethyl 2,3-di-O-benzoyl-4-C-vinyl-6-O-benzyl-β-D-galactopyranoside 
• 174149-24-7 2-(trimethylsilyl)ethyl 2,3-di-O-benzoyl-6-O-benzyl-β-D-glucopyranoside 
• 174149-27-0 2-(trimethylsilyl)ethyl 2,3-di-O-benzoyl-4-C-(hydroxymethyl)-6-O-benzyl-β-D-galactopyranoside 
• 174149-23-6 2-(trimethylsilyl)ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranoside 
• 117253-03-9 2-(trimethylsilyl)ethyl 4,6-O-benzylidene-β-D-glucopyranoside 
• 81336-89-2 (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(2-(trimethylsilyl)ethoxy)tetrahydro-2H-pyran-3,4,5-triol 
• 81342-44-1 (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(2-(trimethylsilyl)ethoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate 
• 1125-88-8 benzaldehyde dimethyl acetal 

Relevant academic research and scientific papers

Synthesis of a sialyl Lewis x mimic with fixed carboxylic acid group: Chemical approach toward the elucidation of the bioactive conformation of sialyl Lewis x

The relation of the solution and bioactive conformation of sialyl Lewis x (sLe(x)) has been addressed by chemical means. To mimic the preferred solution conformation of sLe(x) 1, the more rigid analog 2 has been designed and synthesized. The sialic acid r