126330-75-4

Upstream product

• 2127-03-9 2,2'-dipyridyldisulphide 
• 210426-02-1 2,3,4-tri-O-benzyl-L-rhamnopyranose 
• 100-39-0 benzyl bromide 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 162118-38-9 (3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-6-methyltetrahydro-2H-pyran-2-ol 
• 136984-94-6 2-pyridyl 2,3,4-tri-O-acetyl-1-thio-α/β-L-rhamnoyranoside 
• 2637-34-5 2-Sulfanylpyridine 

Downstream Products

• 126330-72-1 (3aR,4R,6S,7S,7aR)-4-Methoxy-2,2,6-trimethyl-7-((2S,3R,4R,5S,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 64694-29-7 1,2:5,6-di-O-isopropylidene-α-D-glucofuranos-3-yl 2,3,4-tri-O-benzyl-α-L-fucopyranose 
• 71672-13-4 2,3,4-tri-O-benzyl-α-L-fucopyanosyl-(1->6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 126330-71-0 6-O-(2,3,4-tri-O-benzyl-L-rhamnopyranosyl)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 

Relevant academic research and scientific papers

Stereoselective synthesis of α-linked saccharides by use of per O-benzylated 2-pyridyl 1-thio hexopyranosides as glycosyl donors and methyl iodide as an activator

A new, practical, stereoselective glycosidation methodology is described where per O-benzylated 2-pyridyl 1-thio-α/β-hexopyranosyl donors of D-gluco-(1), D-galacto- (2), D-manno- (3) and L-rhamno- (4) configurations have been efficiently coupled with dive

A MILD GENERAL METHOD FOR THE SYNTHESIS OF α-LINKED DISACCHARIDES

Stereoselective α-glycosylations may be achieved using stable 2-pyridyl thioglycosides (anomeric mixture) having a non-participating 2-substituent as glycosyl donor and methyl iodide as an activator.