Literature DB >> 22658363

Regioselective synthesis and antimicrobial studies of ester linked 1,4-disubstituted 1,2,3-bistriazoles.

Kashmiri Lal1, Ashwani Kumar, M S Pavan, C P Kaushik.   

Abstract

A series of 1,4-disubstituted 1,2,3-bistriazoles was synthesized via click chemistry by cycloaddition of various bisalkynes with benzyl/2-phenylethyl azide. Synthesized triazoles were characterized by IR, (1)H NMR, (13)C NMR and mass spectral techniques. All the compounds were evaluated for antibacterial/antifungal activities and found to possess moderate to good antimicrobial activities. Further the docking study for the most active compound against DNA Gyrase was also carried out.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22658363     DOI: 10.1016/j.bmcl.2012.05.008

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Synthesis and antimicrobial evaluation of ester-linked 1,4-disubstituted 1,2,3-triazoles with a furyl/thienyl moiety.

Authors:  C P Kaushik; Raj Luxmi; Dharmendra Singh; Ashwani Kumar
Journal:  Mol Divers       Date:  2016-11-29       Impact factor: 2.943

Review 2.  Synthesis of bi- and bis-1,2,3-triazoles by copper-catalyzed Huisgen cycloaddition: A family of valuable products by click chemistry.

Authors:  Zhan-Jiang Zheng; Ding Wang; Zheng Xu; Li-Wen Xu
Journal:  Beilstein J Org Chem       Date:  2015-12-11       Impact factor: 2.883

  2 in total

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