112348-35-3

Upstream product

• 98-88-4 benzoyl chloride 
• 112348-34-2 benzyl 4-bromo-4-deoxy-2-O-benzoyl-β-L-lyxopyranoside 
• 18403-20-8 benzyl 2-O-benzoyl-α-D-xylopyranoside 
• 112348-33-1 benzyl 2-O-benzoyl-α-D-erythro-pent-3-enopyranoside 
• 18403-12-8 benzyl β-D-xylopyranoside 

Downstream Products

• 112348-39-7 benzyl 4-<2-(phenylsulfonyl)ethyl>-4-deoxy-2,3-di-O-benzoyl-β-L-lyxopyranoside 
• 112348-38-6 benzyl 4-deoxy-2,3-di-O-benzoyl-β-L-lyxopyranoside 
• 112348-44-4 C₃₀H₃₀O₈S 
• 112348-43-3 1-<5-<2-(phenylsulfonyl)ethyl>-2α,3β,4β,5α-tetrahydro-3,4-di-O-benzoyl-2H-pyran-2-yl>-2-propanone 
• 112348-41-1 C₂₇H₂₆O₈S 
• 89824-53-3 benzyl 4-<2-(phenylsulfonyl)ethyl>-4-deoxy-2,3-O-isopropylidene-β-L-lyxopyranoside 
• 112348-40-0 benzyl 4-<2-(phenylsulfonyl)ethyl>-4-deoxy-β-L-lyxopyranoside 

Relevant academic research and scientific papers

An Approach to Pseudomonic Acids from D-Xylose

The four contiguous chiral centers present in pseudomonic acid C are constructed in an efficient way from D-xylose.The key steps involve a highly selective intermolecular radical reaction between benzyl 4-bromo-4-deoxy-2,3-di-O-benzoyl-β-L-lyxopyranoside (9) and phenyl vinyl sulfone for incorporating the lower appendage and a stereoselective intramolecular Michael addition to achieve the correct stereochemistry at the anomeric site.

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