872333-46-5

Upstream product

• 861819-33-2 ethyl 4-azido-3-O-benzyl-4,6-dideoxy-1-thio-β-D-glucopyranoside 
• 598-21-0 2-Bromoacetyl bromide 
• 876345-23-2 1-O-acetyl-4-azido-3-O-benzyl-2-O-bromoacetyl-4,6-dideoxy-D-glucopyranoside 
• 75-08-1 ethanethiol 
• 861819-27-4 methyl 4-azido-3-O-benzyl-4,6-dideoxy-α-D-glucopyranoside 
• 876345-22-1 methyl 4-azido-3-O-benzyl-2-O-bromoacetyl-4,6-dideoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of the β anomer of the spacer-equipped tetrasaccharide side chain of the major glycoprotein of the Bacillus anthracis exosporium

The β glycoside of the tetrasaccharide sequence β-Ant-(1→3)- α-l-Rhap-(1→3)-α-l-Rhap-(1→2)-l-Rhap, whose aglycon allows conjugation to proteins, was synthesized for the first time. A stepwise synthetic approach was applied with thioglycosides as glycosyl

Immunogens related to the synthetic tetrasaccharide side chain of the Bacillus anthracis exosporium

The known methyl 2-O-acetyl-3,4-di-O-benzyl-1-thio-α-l-rhamnopyranoside (3) was converted to the corresponding 5-methoxycarbonylpentyl glycoside 4 which was deacetylated. The product 5 was used as the initial glycosyl acceptor to construct two trirhamnosi

Synthesis of the tetrasaccharide side chain of the major glycoprotein of the Bacillus anthracis exosporium

An α-glycoside of the tetrasaccharide sequence β-Ant-(1 → 3)-α-L-Rhap-(1 → 3)-α-L-Rhap-(1 → 2)-α-L-Rhap whose aglycon allows conjugation to suitable carriers was synthesized. The NMR characteristics of the compound are virtually identical with those of th