Studies on epimeric D-xylo-and D-lyxo -tetritol-1-yl-2-phenyl-2 H-1,2,3- triazoles. Synthesis and anomeric configuration of 4-(α- and β-D- threofuranosyl)- 2-phenyl-2H-1,2,3- triazole C-nucleoside analogs

Article abstract of DOI:10.1080/15257770008033034

Treatment of 4-(D-xylo-tetritol-1-yl)-2-phenyl-2H-1,2,3-triazole (1) with one mole equivalent of tosyl chloride in pyridine solution, afforded the C-nucleoside analog; 4-(β-D-threofuranosyl)-2-phenyl-2H-1,2,3-triazole (2) in 55% yield, as well as the bypr

Full text of DOI:10.1080/15257770008033034

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Nucleosides, Nucleotides and Nucleic
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Studies on Epimeric D-xylo-and D-
lyxo-Tetritol-yl-2-phenyl-2H-1,2,3-
triazoles. Synthesis and Anomeric
Configuration of 4-(α- and β-D-
Threofuranosyl)-2-phenyl-2H-1,2,3-
triazole C-Nucleoside Analogs
Mohammed A. E. Sallam a , Farida F. Louis a & John M. Cassady b
a Chemistry Department, Faculty of Science , Alexandria
University , Alexandria, Egypt
b College of Pharmacy, The Ohio State University , Columbus,
OH, 43210
Published online: 24 Sep 2006.
To cite this article: Mohammed A. E. Sallam , Farida F. Louis & John M. Cassady (2000) Studies
on Epimeric D-xylo-and D-lyxo-Tetritol-yl-2-phenyl-2H-1,2,3-triazoles. Synthesis and Anomeric
Configuration of 4-(α- and β-D-Threofuranosyl)-2-phenyl-2H-1,2,3-triazole C-Nucleoside Analogs,
Nucleosides, Nucleotides and Nucleic Acids, 19:5-6, 941-954, DOI: 10.1080/15257770008033034
To link to this article: http://dx.doi.org/10.1080/15257770008033034
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