56933-03-0

Upstream product

• 98-88-4 benzoyl chloride 
• 359407-34-4 1,2-di-O-benzoyl-α-L-arabinopyranose 
• 144217-03-8 1,2-di-O-benzoyl-3,4-O-isopropylidene-α-L-arabinopyranose 
• 87-72-9 L-(+)-arabinose 

Downstream Products

• 82040-49-1 1,2,3-tri-O-benzoyl-4-O-trifluoromethanesulphonyl-β-L-arabinopyranose 
• 82040-50-4 1,2,3-tri-O-benzoyl-4-S-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-4-thio-α-D-xylopyranose 
• 359407-40-2 C₅₆H₅₂O₁₉S₂ 
• 359407-49-1 C₆₉H₆₆O₂₃S₃ 
• 943621-49-6 1,2,3-tri-O-benzoyl-4-deoxy-4-fluoro-α-D-xylopyranose 

Relevant academic research and scientific papers

4-Deoxy-4-fluoro-xyloside derivatives as inhibitors of glycosaminoglycan biosynthesis

Various 4-deoxy-4-fluoro-xylosides were prepared using click chemistry for evaluating their potential utility as inhibitors of glycosaminoglycan biosynthesis. 2,3-Di-O-benzoyl-4-deoxy-4-fluoro-β-d-xylopyranosylazide, obtained from l-arabinopyranose by six

Stereoselective synthesis of thioxylooligosaccharides from S-glycosyl isothiourea precursors

A stereoselective synthesis of thioxylo-di-, -tri-, -tetra- and -penta-saccharides from S-glycosyl isothiourea precursors is described. The synthesis was performed starting from 2,3,4-tri-O-acetyl-β-D-xylopyranosyl isothiouronium bromide using a triethylamine promoted reaction with 1,2,3-tri-O-benzoyl-4-O-trifluoromethanesulphonyl-β-L-arabinopyranose. The resulting 4-thioxylobiose was then converted into the corresponding isothiouronium bromide and used for the synthesis of 4,4′-dithioxylotriose. Higher homologues of the series and their α-methyl glycosides were also prepared.