365534-75-4

Upstream product

• 365535-43-9 2'-(benzyloxycarbonyl)benzyl 4,6-O-benzylidene-α-D-mannopyranoside 
• 365535-62-2 2-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 13242-53-0 acetobromomannose 
• 365535-42-8 2-(benzyloxycarbonyl)benzyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 365534-59-4 2'-(benzyloxycarbonyl)benzyl α-D-mannopyranoside 
• 365534-57-2 2-(hydroxymethyl)benzoic acid benzyl ester 
• 365535-64-4 2-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranoside 
• 3282-30-2 pivaloyl chloride 

Downstream Products

• 365535-17-7 2-(hydroxycarbonyl)benzyl (2,3-di-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl)-(1->6)-3,4-di-O-benzyl-2-O-pivaloyl-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

Glycosylation with 2′-carboxybenzyl glycosides as glycosyl donors: Scope and application to the synthesis of a tetrasaccharide

Glycosylation of 2′-carboxybenzyl (CB) 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside (3), CB 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside (4), and CB 2,3-di-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside (5) as glycosyl donors with various glycosyl acceptors p