862898-12-2

Upstream product

• 16977-78-9 2'-bromoethyl-2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 707-07-3 orthobenzoic acid trimethyl ester 
• 530-26-7 D-Mannose 
• 110891-64-0 2'-bromoethyl-α-D-mannopyranoside 
• 211801-79-5 4-methylphenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-mannopyranoside 
• 282094-71-7 2-bromoethyl 2,4-di-O-benzoyl-α-D-mannopyranoside 
• 121238-27-5 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl trichloroimidate 
• 4163-65-9 per-O-acetyl-α-D-mannopyranose 

Downstream Products

• 862898-13-3 2-S-acetylthioethyl 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 
• 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 
• 862898-14-4 2-azidoethyl 3,6-di-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-2,4-di-O-benzoyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

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

From solution phase to "on-column" chemistry: Trichloroacetimidate-based glycosylation promoted by perchloric acid-silica

Activation of ester-protected glycosyl trichloroacetimidate donors by perchloric acid immobilized on silica afforded 1,2-trans disaccharides in 60-90% yields. Applying this approach to one-pot sequential glycosylation resulted in efficient syntheses of th

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.