862898-14-4

Upstream product

• 862898-12-2 2-bromoethyl 3,6-di-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2,4-di-O-benzoyl-α-D-mannopyranoside 
• 211801-79-5 4-methylphenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-mannopyranoside 
• 4163-65-9 per-O-acetyl-α-D-mannopyranose 
• 282094-71-7 2-bromoethyl 2,4-di-O-benzoyl-α-D-mannopyranoside 
• 110891-64-0 2'-bromoethyl-α-D-mannopyranoside 
• 16977-78-9 2'-bromoethyl-2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 

Downstream Products

• 862898-15-5 2-aminoethyl 3,6-di-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2,4-di-O-benzoyl-α-D-mannopyranoside 
• 862898-16-6 N-(2-[3,6-di-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2,4-di-O-benzoyl-α-D-mannopyranosyloxy]ethyl)thioctamide 

Relevant academic research and scientific papers

Glycosylation reactions with 'disarmed' thioglycoside donors promoted by N-iodosuccinimide and HClO4-silica

Glycosylation of 'disarmed' thioglycosides promoted by NIS in the presence of HClO4 immobilized on silica compares very favourably with the accepted NIS-TfOH procedure.

Thioctic acid amides: Convenient tethers for achieving low nonspecific protein binding to carbohydrates presented on gold surfaces

The thioctic acid amides of 2′-aminoethyl α-D-mannopyranoside and 2′-aminoethyl α-1,3-D-mannopyranosyl (α-1,6-D- mannopyranosyl)-α-D-mannopyranoside presented on both planar and nanoparticle gold surfaces give higher specific and lower non-specific protei