Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60720
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dc.contributor.authorTiwari, Shailendra-
dc.contributor.authorSingh, Vishal Kumar-
dc.contributor.authorRahmani, Shahla-
dc.contributor.authorAhmad, Akeel-
dc.contributor.authorBegum, Kahkashan-
dc.date.accessioned2022-10-21T04:51:56Z-
dc.date.available2022-10-21T04:51:56Z-
dc.date.issued2022-10-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60720-
dc.description1097-1102en_US
dc.description.abstractA series of thiazolo [4,5-b]- pyridine-6-carbonitriles scaffold have been synthesized conveniently and smoothly in a single step in good yields. These compounds have been screened for their antibacterial and antifungal activity against different pathogenic strains of bacteria and fungi. The minimum inhibitory concentration (MBC) and minimum fungicidal concentration (MFC) have been determined for the test compounds as well as for reference standards. Compounds 3c, 3d, 3e, 3f, 4c, 4d, 4e and 4f have shown good antibacterial as well as antifungal activity.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.61(10) [Oct 2022]en_US
dc.subject3-Benzyl-4-thiazolidinon-2-thioneen_US
dc.subjectCarbonitrileen_US
dc.subjectAntibacterialen_US
dc.subjectantifungal activityen_US
dc.titleOne-pot Michael addition and cyclo-elimination cascade synthesis of thiazolo-[4,5-b]pyridin-6-carbonitrile scaffolden_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i10.59435en_US
Appears in Collections:IJC Vol.61(10) [Oct 2022]

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