359686-59-2

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 359686-52-5 p-[2-(benzyloxycarbonyl)ethyl]phenyl 3,6-di-O-pivaloyl-β-D-galactopyranoside 
• 501-97-3 4-hydroxyphenylpropionic acid 
• 31770-76-0 3-(4-hydroxyphenyl)propionic acid benzyl ester 
• 3282-30-2 pivaloyl chloride 
• 100-39-0 benzyl bromide 
• 359686-45-6 p-[2-(benzyloxycarbonyl)ethyl]phenyl β-D-galactopyranoside 
• 359686-41-2 p-[2-(benzyloxycarbonyl)ethyl]phenyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 

Downstream Products

• 359686-64-9 p-[2-(benzyloxycarbonyl)ethyl]phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359686-69-4 p-[2-(benzyloxycarbonyl)ethyl]phenyl 4-O-acetyl-3,6-di-O-pivaloyl-2-O-trifluoromethylsulfonyl-β-D-glucopyranoside 
• 359687-25-5 p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2-acetamido-2-deoxy-4-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359687-32-4 p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359687-29-9 p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 4-O-acetyl-2-deoxy-3,6-di-O-pivaloyl-β-D-arabino-hexopyranoside 
• 359686-95-6 p-[2-(benzyloxycarbonyl)ethyl]phenyl 2-acetamido-2-deoxy-4-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359686-74-1 p-[2-(benzyloxycarbonyl)ethyl]phenyl 4-O-acetyl-2-azido-2-deoxy-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359687-05-1 p-(2-carboxyethyl)phenyl 2-acetamido-2-deoxy-4-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359686-81-0 p-[2-(benzyloxycarbonyl)ethyl]phenyl 4-O-acetyl-2-deoxy-3,6-di-O-pivaloyl-β-D-arabino-hexopyranoside 
• 359687-00-6 p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359687-39-1 p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2-acetamido-2-deoxy-β-D-mannopyranoside 
• 359687-15-3 p-(2-carboxyethyl)phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359687-10-8 p-(2-carboxyethyl)phenyl 4-O-acetyl-2-deoxy-3,6-di-O-pivaloyl-β-D-arabino-hexopyranoside 
• 359687-48-2 p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 2-deoxy-2-fluoro-β-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of new glycopolymers containing β-d-mannopyranose, and c-2-substituted β-d-mannopyranose residues as a new class of inhibitor

New styryl monomers containing β-D-mannopyranose, 2-acetamido-2-deoxy-β-D-mannopyranose, 2-deoxy-2-fluoro-β-D-mannopyranose, and 2-deoxy-β-D-arabino-hexopyranose on their side chains, were efficiently synthesized as a new class of a potent inhibitor resistant to exo-α-mannosidase digestion. The binding affinity of the carbohydrate polymers obtained from those mannopyranosyl styryl monomers by radical polymerization with Concanavalin A were evaluated. A binding assay indicated that the multivalency effect and the affinity enhancement attained by modification at the C-2 position of the β-D-mannopyranoside residue resulted in the.