365534-59-4

Upstream product

• 100-39-0 benzyl bromide 
• 87-41-2 2-benzofuran-1(3H)-one 
• 13242-53-0 acetobromomannose 
• 365534-57-2 2-(hydroxymethyl)benzoic acid benzyl ester 
• 365535-42-8 2-(benzyloxycarbonyl)benzyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 

Downstream Products

• 365535-43-9 2'-(benzyloxycarbonyl)benzyl 4,6-O-benzylidene-α-D-mannopyranoside 
• 365535-44-0 2-(benzyloxycarbonyl)benzyl 4,6-O-cyclohexylidene-α-D-mannopyranoside 
• 365535-48-4 2-(benzyloxycarbonyl)benzyl 2,3-O-cyclohexylidene-α-D-mannopyranoside 
• 365534-75-4 2'-(benzyloxycarbonyl)benzyl 3,4-di-O-benzyl-2-O-pivaloyl-α-D-mannopyranoside 
• 365535-64-4 2-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranoside 
• 365535-62-2 2-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 365534-66-3 2-(hydroxycarbonyl)benzyl 4,6-O-benzoyl-2,3-O-cyclohexylidene-α-D-mannopyranoside 
• 365534-61-8 2-(benzyloxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 365534-65-2 2-(hydroxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-cyclohexylidene-α-D-mannopyranoside 
• 365534-69-6 2-(hydroxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranoside 
• 365534-63-0 2-(hydroxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 365535-50-8 2-(benzyloxycarbonyl)benzyl 4,6-di-O-benzoyl-2,3-O-cyclohexylidene-α-D-mannopyranoside 
• 365535-46-2 2-(benzyloxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-cyclohexylidene-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of the tetrasaccharide repeat unit of the O-antigen polysaccharide from Escherichia coli O77 employing the 2′-carboxybenzyl glycoside

The synthesis of the suitably protected form (1) of the tetrasaccharide repeat unit, →2)-α-D-Manp-(1→2)-β-D-Manp-(1→3)- α-D-GlcpNAc-(1→6)-α-D-Manp-(1→ (A), of the O-antigen polysaccharide of the lipopolysaccharide from Escherichia coli O77 has been accomp

2-(Hydroxycarbonyl)benzyl glycosides: A novel type of glycosyl donors for highly efficient β-mannopyranosylation and oligosaccharide synthesis by latent-active glycosylation

2-(Benzyloxycarbonyl)benzyl (BCB) glycosides were prepared by coupling of the corresponding tetraacetylglycosyl bromides and benzyl 2-(hydroxymethyl)benzoate. The BCB glycosides were converted almost quantitatively into the corresponding 2-(hydroxycarbony