402759-08-4

Upstream product

• 402758-82-1 methyl 2-O-benzyl-α-D-arabinofuranoside 
• 402758-78-5 p-cresyl 2-O-benzoyl-3,5-di-O-benzyl-1-thio-α-D-arabinofuranoside 
• 1239914-90-9 C₃₃H₃₂O₅S 
• 402758-86-5 methyl 2-O-benzoyl-3,5-di-O-benzyl-α-D-arabinofuranoside 
• 329360-22-7 1-O-methyl-3,5-di-O-benzyl-α-D-arabinofuranose 
• 164454-52-8 methyl 3,5-O-(tetraisopropylsiloxane-1,3-diyl)-α-D-arabinofuranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 402759-10-8 methyl 2-O-benzyl-3-O-(3,5-di-O-benzyl-α-D-arabinofuranosyl)-5-O-(3,5-di-O-benzyl-2-O-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 402759-11-9 methyl 2-O-benzyl-5-O-(3,5-di-O-benzyl-α-D-arabinofuranosyl)-3-O-(3,5-di-O-benzyl-2-O-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-α-arabinofuranosyl)-α-D-arabinofuranoside 
• 402759-09-5 methyl 3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->3)-[3,5-di-O-benzyl-α-D-arabinofuranosyl-(1->5)]-2-O-benzyl-α-D-arabinofuranoside 

Relevant academic research and scientific papers

β-selective arabinofuranosylation using a 2,3-o-xylylene-protected donor

Reported is a novel stereoselective β-arabinofuranosylation that makes use of a conformationally restricted 2,3-O-xylylene-protected arabinofuranosyl donor. Optimization of the reaction conditions showed that factors including the structure of the accepto

Arabinofuranosides from mycobacteria: Synthesis of a highly branched hexasaccharide and related fragments containing β-arabinofuranosyl residues

The synthesis of 11 oligosaccharides (4-14) containing β-arabinofuranosyl residues is reported. The glycans are all fragments of two polysaccharides, arabinogalactan and lipoarabinomannan, which are found in the cell wall complex of mycobacteria. In the preparation of the targets, the key step was a low-]temperature glycosylation reaction that installed the β-arabinofuranosyl residues with good to excellent stereocontrol.