365535-64-4

Upstream product

• 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 
• 100-39-0 benzyl bromide 
• 87-41-2 2-benzofuran-1(3H)-one 
• 365535-43-9 2'-(benzyloxycarbonyl)benzyl 4,6-O-benzylidene-α-D-mannopyranoside 
• 3282-30-2 pivaloyl chloride 
• 365535-62-2 2-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 

Downstream Products

• 365534-69-6 2-(hydroxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-2-O-pivaloyl-α-D-mannopyranoside 
• 365534-75-4 2'-(benzyloxycarbonyl)benzyl 3,4-di-O-benzyl-2-O-pivaloyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

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

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