228563-48-2

Upstream product

• 228563-40-4 thexyldimethylsilyl O-(2,3,4-tri-O-acetyl-6-O-benzyl-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-2-azido-6-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 228563-39-1 thexyldimethylsilyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-2-azido-6-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 171754-66-8 O-(2,3,4-tri-O-acetyl-6-O-benzyl-α-D-galactopyranosyl) trichloroacetimidate 
• 157488-87-4 thexyldimethylsilyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-2-azido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 157488-91-0 thexyldimethylsilyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 157488-88-5 thexyldimethylsilyl 2-azido-2-deoxy-β-D-glucopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 67-64-1 acetone 
• 228563-47-1 thexyldimethylsilyl O-(6-O-benzyl-β-D-galactopyranosyl)-(1->4)-[(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)]-2-azido-6-O-benzyl-2-deoxy-β-D-glucopyranoside 

Relevant academic research and scientific papers

Efficient synthesis of lactoneo series antigen Lewis Y (Ley)

The synthesis of glycosphingolipid Lewis Y (1) could be efficiently carried out, based on the connection of building blocks 2-7. Reaction of fucosyl donor 2 with azidoglucose derivative 4 as acceptor gave α(1-3)-linked disaccharide 8, which was transforme