Studies on the dehydrative cyclization of epimeric 4-(L-xylo and L-lyxo-tetritol-1-yl)-2-phenyl-2H-1,2,3-triazoles. Circular dichroism and NMR assignment of the formed anomeric C-nucleoside L-threofuranosyl triazole analogs |
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| Authors: | Sallam Mohammed A E Louis Farida F |
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| Affiliation: | Chemistry Department, Faculty of Science, Alexandria University, Alexandria, Egypt. maesallam@yahoo.com |
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| Abstract: | Dehydrative cyclization of epimeric 4-(L-xylo- and L-lyxo-tetritol-1-yl)-2-phenyl-2H-1,2,3-triazoles afforded the anomeric alpha and beta-L-threofuranosyl analogs. The anomeric configuration of the formed anomeric C-nucleoside analogs was determined by circular dichroism and NMR spectroscopy. |
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| Keywords: | C‐nucleosides 1,2,3‐triazoles circular dichroism anomeric configuration NOE |
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