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Research Article
2 (
2
); 53-60

Synthesis of New 1,2,3-Triazole Glycosides-Based Quinoline System via Click Cycloaddition

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This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
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This article was originally published by Qassim University and was migrated to Scientific Scholar after the change of Publisher.

Abstract

The impact of novel compounds based small heterocyclic rings with important bioactivities promotes further research for designing and synthesizing new hybrid molecules. In the current investigation, new azido quinoline derivative has been synthesized from the commercially available 8-hydroxyquinoline. The obtained azido derivative was exploited via click chemistry to access three new 1,2,3-triazole glycosides by applying click chemistry reaction strategy. The newly synthesized compounds have been characterized by their spectral and analytical data involving 1H, 13C NMR and IR. The anticancer activity of the synthesized products were evaluated agains a pannel of human cancer cell lines and the results were formulated in the form of IC50 and percentage inhibition values.  


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