91602-37-8

Upstream product

• 71204-45-0 benzyl 2,3-anhydro-4-O-trifluoromethanesulfonyl-β-L-ribopyranoside 

Downstream Products

• 71204-45-0 benzyl 2,3-anhydro-4-O-trifluoromethanesulfonyl-β-L-ribopyranoside 
• 113727-15-4 Benzyl-2,3-anhydro-4-desoxy-4-glycinbenzylester>-α-D-lyxopyranosid 
• 109304-20-3 Benzyl-4-(L-alanino-benzylester)-2,3-anhydro-4-desoxy-α-D-lyxopyranosid 
• 109304-18-9 Benzyl-3,4-didesoxy-3,4-(epialanino-benzylester)-α-D-arabinopyranosid 
• 108292-74-6 Benzyl 2,3-Anhydro-4-<4-(tert-butyloxycarbonyl)phenylamino>-4-deoxy-α-D-lyxopyranoside 

Relevant academic research and scientific papers

Classical Synthesis of a New Class of Compounds via Coupling of Sugars and Amino Acids

A new class of pharmacologically interesting compounds has been synthesized through a novel SN2 displacement of the CF3SO2 group in benzyl 2,3-anhydro-4-trifluoromethylsulphonyl-α-D-ribopyranoside (1) and its β-L-isomer (2), by a variety of suitably protected naturally occurring amino acids: the reaction pathway also provides an efficient route to benzyl 2,3-anhydro-β-L- and -α-D-lyxopyranosides .