210295-20-8

Upstream product

• 216776-90-8 Chloro-acetic acid (2R,3R,4S,5S,6R)-3,5-bis-benzyloxy-6-phenylsulfanyl-4-((2R,3S,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-ylmethyl ester 
• 4163-65-9 per-O-acetyl-α-D-mannopyranose 
• 210295-04-8 phenyl 3,6-di-O-pivaloyl-1-thio-α-D-mannopyranoside 
• 2936-70-1 (2R,3S,4S,5S,6R)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 22860-22-6 2,3,4,6-tetra-O-acetyl-α-D-mannopyranose 
• 216776-70-4 phenyl 2,4-di-O-benzyl-6-O-chloroacetyl-1-thio-α-D-mannopyranoside 
• 210295-06-0 phenyl 2,4-di-O-benzyl-1-phenylthio-α-D-mannopyranoside 
• 121238-27-5 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl trichloroimidate 

Downstream Products

• 216777-16-1 O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1-2)-O-(3,4,6-tri-O-acetyl-α-D-mannopyranosyl)-(1-6)-[O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1-3)]-2,4-di-O-benzyl-D-mannopyranosyl trichloroacetimidate 

Relevant academic research and scientific papers

A short, efficient synthesis of the octamannan residue of high mannose type sugar chains

An efficient route for the synthesis of octamannan 1, found in high mannose type sugar chains, is described. To construct octasaccharide 1 by as few synthetic steps as possible, we employed a chemoenzymatic strategy: the enzymatic synthesis of oligosaccha

Chemoenzymatic synthesis of the branched oligosaccharides which correspond to the core structures of N-linked sugar chains

Synthetic routes are described to a partial structure common to all high mannose-type sugar chains and complex-type sugar chains based on a chemoenzymatic strategy which incorporates, (a) enzymatic synthesis of oligosaccharide blocks using glycosidases, a