197087-06-2

Upstream product

• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 14687-15-1 methyl L-fucopyranoside 
• 152554-45-5 β-methyl 2,3,4-tri-O-(4-chlorobenzyl)-6-deoxy-L-galactopyranoside 
• 108-24-7 acetic anhydride 

Downstream Products

• 197087-16-4 C₆₅H₆₈Cl₃NO₂₀ 
• 197087-12-0 2-{(2R,3R,4R,5S,6R)-2-Allyloxy-6-benzyloxymethyl-5-hydroxy-4-[(2S,3S,4R,5R,6S)-3,4,5-tris-(4-chloro-benzyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-3-yl}-isoindole-1,3-dione 
• 197087-09-5 2-{(2R,4aR,6R,7R,8R,8aS)-6-Allyloxy-2-phenyl-8-[(2S,3S,4R,5R,6S)-3,4,5-tris-(4-chloro-benzyloxy)-6-methyl-tetrahydro-pyran-2-yloxy]-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl}-isoindole-1,3-dione 

Relevant academic research and scientific papers

Para-Chlorobenzyl protecting groups as stabilizers of the glycosidic linkage: Synthesis of the 3-O-Sulfated lewis X trisaccharide

Thr 3'O-sulfated trisacchande Lewis x (1) and unsulfated Lewis x (2) have been synthesized using a route that highlights a more facile regio selective benzylidene ring-opening procedure and the employment of chlorobenzyl groups as a way of strengthening the acid-labile α-fucose linkage.