112482-99-2

Upstream product

• 98-88-4 benzoyl chloride 
• 112483-13-3 benzyl 3-cyano-3-deoxy-α-D-xylopyranoside 
• 151-50-8 potassium cyanide 
• 61134-24-5 Benzyl 2,3-anhydro-α-D-ribopyranoside 
• 18403-20-8 benzyl 2-O-benzoyl-α-D-xylopyranoside 
• 112482-93-6 benzyl 3,4-dideoxy-α-D-glycero-pent-3-enopyranoside 
• 112482-94-7 benzyl 3,4-anhydro-α-D-ribopyranoside 
• 112348-36-4 benzyl 4-bromo-4-deoxy-β-L-lyxopyranoside 
• 112348-33-1 benzyl 2-O-benzoyl-α-D-erythro-pent-3-enopyranoside 
• 112348-34-2 benzyl 4-bromo-4-deoxy-2-O-benzoyl-β-L-lyxopyranoside 

Relevant academic research and scientific papers

Ring opening reactions of benzyl 2,3-anhydro-α-D-ribopyranoside with nucleophiles

Nucleophilic ring opening reactions of benzyl 2,3 anhydro-α-D-ribopyranoside with different nucleophiles resulted in exclusive formation of 3-substituted-3-deoxyxylose derivatives in good yields. The regiochemical outcome of the ring opening reaction is c

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