28708-23-8

Upstream product

• 18484-40-7 <2-Hydroxy-pyridin>-O-β-D-glucosid 
• 98-88-4 benzoyl chloride 
• 22918-00-9 2-hydroxypyridine silver salt 
• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 17430-62-5 2-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)oxy]pyridine 
• 142-08-5 2-Pyridone 
• 339276-12-9 2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl 1-(N-phenyl)-2,2,2-trifluoroacetimidate 

Downstream Products

• 118579-76-3 methyl 4-O-(2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 128503-39-9 methyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl)-α-D-glucopyranoside 

Relevant academic research and scientific papers

2-Pyridyl glycoside: An alternative glycosyl donor in preactivation protocol

2-Pyridyl glycosides have been identified to be powerful glycosyl donors for the preactivation-based oligosaccharide synthesis. By using stoichiometric amount of Tf2O, the 2-pyridyl glycosides were pre-activated, which subsequently underwent gl

Effective synthesis of nucleosides with glycosyl trifluoroacetimidates as donors

Glycosyl trifluoroacetimidates have been disclosed to be effective glycosyl donors for the synthesis of nucleosides; the present N-glycosylation protocol requires only a catalytic amount of TMSOTf as promoter and proceeds smoothly at room temperature.