1083195-76-9

Upstream product

• 31106-82-8 2-(bromomethyl)pyridine hydrobromide 
• 180187-58-0 ethyl 3,4,6-tri-O-benzyl-1-thio-β-D-glucopyranoside 

Downstream Products

• 873093-23-3 methyl 2,3,4-tri-O-benzyl-6-O-(3,4,6-tri-O-benzyl-2-O-picolinyl-β-D-glucopyranosyl)-α-D-glucopyranoside 
• 1083195-86-1 O-(2,3,4-tri-O-benzyl-2-O-picolyl-β-D-glucopyranosyl)-(1-3)-1,2:5,6-di-O-isopropylidenene-α-D-glucofuranoside 

Relevant academic research and scientific papers

How the arming participating moieties can broaden the scope of chemoselective oligosaccharide synthesis by allowing the inverse armed-disarmed approach

(Chemical Equation Presented) A new method for stereocontrolled glycosylation and chemoselective oligosaccharide synthesis has been developed. It has been determined that complete 1,2-trans selectivity can be achieved with the use of a 2-O-picolyl moiety,