1242261-26-2Relevant academic research and scientific papers
Regioselective [3+2] cycloaddition of chalcones with a sugar azide: Easy access to 1-(5-deoxy-d-xylofuranos-5-yl)-4,5-disubstituted-1H-1,2,3-triazoles
Singh, Nimisha,Pandey,Tripathi, Rama P.
experimental part, p. 1641 - 1648 (2010/10/04)
[3+2] Cycloaddition of 5-azido-5-deoxy-1,2-O-isopropylidene-α-d- xylofuranose with 1,3-diphenyl-prop-3-enones, followed by oxidation of the intermediate triazolines in a tandem manner, led to the regioselective formation of 4-benzoyl-1-(5-deoxy-1,2-O-isopropylidene-α-d-xylofuranos-5-yl)-5- phenyl-1H-1,2,3-triazoles in moderate to good yields.
