126330-72-1

Upstream product

• 116514-50-2 ethyl 2,3,4-tri-O-benzyl-1-thio-β-L-fucopyranoside 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-L-rhamnoside 
• 33639-77-9 perbenzyl fucosyl bromide 
• 126330-69-6 2-pyridyl 2,3,4-tri-O-benzyl-1-thio-α,β-L-rhamnopyranoside 
• 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 
• 59055-61-7 2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl bromide 
• 136984-94-6 2-pyridyl 2,3,4-tri-O-acetyl-1-thio-α/β-L-rhamnoyranoside 

Relevant academic research and scientific papers

A Mechanistic Probe into 1,2-cis Glycoside Formation Catalyzed by Phenanthroline and Further Expansion of Scope

Phenanthroline, a rigid and planar compound with two fused pyridine rings, has been used as a powerful ligand for metals and a binding agent for DNA/RNA. We discovered that phenanthroline could be used as a nucleophilic catalyst to efficiently access high

Diastereoselective sp3C-O Bond Formation via Visible Light-Induced, Copper-Catalyzed Cross-Couplings of Glycosyl Bromides with Aliphatic Alcohols

Copper-catalyzed cross-coupling reactions have become one of the most powerful methods for generating carbon-heteroatom bonds, an important framework of many organic molecules. However, copper-catalyzed C(sp3)-O cross-coupling of alkyl halides with alkyl

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

Synthesis, NMR and Conformational Studies of some 1,4-Linked Disaccharides

Synthesis of, and NMR and conformational studies on the methyl glycosides of some 1,4-linked disaccharides, containing rhamnose and fucose in the methyl glycoside residue, have been performed.The glycosylation shifts were correlated with inter-residue ato

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.