1363497-45-3

Upstream product

• 1248566-22-4 methyl 2-benzyloxycarbonylamino-4,6-O-benzylidene-2-deoxy-α-D-galactopyranoside 
• 1363497-33-9 methyl 2-acetamido-4,6-O-benzylidene-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranoside 
• 3006-58-4 2-carbobenzyloxyamino-2-deoxy-D-galactopyranose 
• 1772-03-8 D-(+)-galactosamine hydrochloride 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 82916-19-6 methyl 2-N-(benzyloxycarbonyl)amino-2-deoxy-α-D-galactopyranoside 
• 1363497-23-7 para-tolyl 2-acetamido-4-O-tert-butyldimethylsilyl-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-1-thio-α-D-galactopyranoside 
• 1363497-42-0 methyl (2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranosyl)-(1->4)-2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranoside 
• 1363497-39-5 methyl (2-acetamido-4-O-tert-butyldimethylsilyl-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranosyl)-(1->4)-2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranoside 
• 1363497-36-2 methyl 2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranoside 
• 1242060-81-6 p-tolyl 2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-1-thio-α-D-galactopyranoside 

Downstream Products

• 1363497-48-6 methyl (2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranosyl)-(1->4)-(2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranosyl)-(1->4)-2-acetamido-6-O-benzyl-2,3-N,O-carbonyl-2-deoxy-α-D-galactopyranoside 
• 1363497-58-8 methyl (2-acetamido-3,4-di-O-acetyl-6-O-benzyl-2-deoxy-α-D-galactopyranosyl)-(1->4)-(2-acetamido-3-O-acetyl-6-O-benzyl-2-deoxy-α-D-galactopyranosyl)-(1->4)-2-acetamido-3-O-acetyl-6-O-benzyl-2-deoxy-α-D-galactopyranoside 

Relevant academic research and scientific papers

A highly α-stereoselective synthesis of oligosaccharide fragments of the VI antigen from salmonella typhi and their antigenic activities

In this paper, a convenient approach to the synthesis of the repeating α-(1→4)-linked N-acetyl galactosaminuronic acid units from the capsular polysaccharide of Salmonella typhi is reported. The exclusively α-stereoselective glycosylation reactions were a