329360-19-2

Upstream product

• 98-88-4 benzoyl chloride 
• 676259-67-9 octyl 2,3-di-O-benzoyl-5-O-triphenylmethyl-α-D-arabinofuranoside 

Downstream Products

• 527681-80-7 n-octyl 5-O-(2,3-anhydro-5-O-benzoyl-α-D-ribofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 685111-72-2 octyl 2,3-di-O-benzoyl-5-O-methyl-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 685111-71-1 octyl 2,3-di-O-benzoyl-5-deoxy-5-fluoro-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 685111-73-3 octyl 5-azido-2,3-di-O-benzoyl-5-deoxy-α-D-arabinofuranosyl-(1->5)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 848436-94-2 octyl 5-O-(2,5-di-O-acetyl-3-O-methyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 848437-04-7 octyl 5-O-(2,5-di-O-acetyl-3-azido-3-deoxy-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 1186016-55-6 octyl 5-O-(4-deoxy-4-thio-2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 1186016-54-5 octyl 5-O-(4-deoxy-4-thio-2,3,5-tri-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranoside 
• 569659-43-4 octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-(5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl))-α-D-arabinofuranoside 
• 569659-40-1 octyl 2,3-di-O-benzoyl-5-O-(2,5-di-O-benzoyl-3-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 569659-38-7 octyl 2,3-di-O-benzoyl-5-O-(2,5-di-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 569659-42-3 octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 569659-37-6 octyl 2,3-di-O-benzoyl-5-O-(2-O-benzoyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside 
• 569659-41-2 octyl 2,3-di-O-benzoyl-5-O-(2,3-di-O-benzoyl-5-O-tert-butyldiphenylsilyl-α-D-arabinofuranosyl)-α-D-arabinofuranoside 

Relevant academic research and scientific papers

2,3-Anhydrosugars in glycoside bond synthesis. Application to the preparation of C-2 functionalized α-D-arabinofuranosides

A novel two-step route has been developed for the synthesis of a panel of oligosaccharides (9-17) containing C-2 functionalized α-D- arabinofuranosyl residues. The first step in this route consists of a highly stereocontrolled glycosylation reaction using