115197-02-9

Upstream product

• 117107-69-4 1,2-Di-O-acetyl-4-azido-4,6-dideoxy-3-O-benzyl-α-D-mannopyranoside 
• 115196-92-4 methyl O-(2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyran... 
• 115196-86-6 methyl O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 115196-81-1 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl bromide 
• 115196-88-8 methyl O-(2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 115196-83-3 methyl 4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 115196-80-0 ethyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)(4-azido-3-O-benzyl-4,6-dideoxy-1-thio-α-D-mannopyranoside 
• 115196-96-8 methyl O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-O-(4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl)-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside 
• 115234-11-2 ethyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-1-thio-α-D-mannopyranoside 
• 115216-48-3 ethyl 4-azido-3-O-benzyl-4,6-dideoxy-1-thio-α-D-mannopyranoside 

Downstream Products

• 115197-07-4 methyl O-(3-O-benzyl-4,6-dideoxy-4-formamido-α-D-mannopyranosyl)-(1->2)-O-(3-O-benzyl-4,6-dideoxy-4-formamido-α-D-mannopyranosyl)-(1->2)-O-(3-O-benzyl-4,6-dideoxy-4-formamido-α-D-mannopyranosyl)-(1->2)-3-O-benzyl-4,6-dideoxy-4-formamido-α-D-manno... 

Relevant academic research and scientific papers

Synthesis of methyl α-glycosides of some higher oligosaccharide fragments of the O-antigen of Vibrio cholerae O1, serotype Inaba and Ogawa

The title oligosaccharides, the tri- through the hexasaccharide in the Inaba series and the penta- and the hexasaccharide in the Ogawa series, have been synthesized using 1-thioglycosides of precursors to 3-O-benzyl-perosamine (4-amino-4,6-dideoxy-D-manno

Synthetic antigenic determinants of the Brucella A polysaccharide: A disaccharide thioglycoside for block synthesis of pentasaccharide and lower homologues of α1,2-linked 4,6-dideoxy-4-formamido-α-D-mannose

Methyl glycosides 13, 18, and 22, which represent potential antigenic determinants of the Brucella A polysaccharide, are the first synthetic analogues of this antigen.Their synthesis was necessitated by crystallographic studies of a Fab combining site obt