112483-17-7

Upstream product

• 112482-94-7 benzyl 3,4-anhydro-α-D-ribopyranoside 
• 112348-36-4 benzyl 4-bromo-4-deoxy-β-L-lyxopyranoside 
• 112348-34-2 benzyl 4-bromo-4-deoxy-2-O-benzoyl-β-L-lyxopyranoside 
• 112348-33-1 benzyl 2-O-benzoyl-α-D-erythro-pent-3-enopyranoside 
• 112482-93-6 benzyl 3,4-dideoxy-α-D-glycero-pent-3-enopyranoside 
• 18403-20-8 benzyl 2-O-benzoyl-α-D-xylopyranoside 
• 61134-24-5 Benzyl 2,3-anhydro-α-D-ribopyranoside 

Downstream Products

• 112483-00-8 benzyl 3-bromo-3-deoxy-2,4-di-O-benzoyl-α-D-xylopyranoside 

Relevant academic research and scientific papers

Regioselective conversion of anhydro sugars into halohydrins and X-ray study

A rapid, easy, regio- and stereoselective synthesis of 3-halo-3-deoxy sugars using titanium tetrahalides is described. To fully confirm the stereochemistry of the synthetic products, the X-ray structure of benzyl 3-chloro-3-deoxy-β-L-xylopyranoside was de

Regiospecific Ring-Opening Reactions of Benzyl 3,4-Anhydro-α-D-ribopyranoside with Nucleophiles: A Systematic Study

Nucleophilic ring-opening reactions of the title compound 6 and its (benzyloxy)methyl ether 27 with different nucleophiles resulted in exclusive formation of 3-substituted 3-deoxyxylose derivatives.On the basis of these experiments, it is postulated that