Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60715
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dc.contributor.authorWalmik, Prabhaker-
dc.date.accessioned2022-10-21T04:34:38Z-
dc.date.available2022-10-21T04:34:38Z-
dc.date.issued2022-10-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60715-
dc.description1134-1138en_US
dc.description.abstractIn the present study, a novel, rapid, improved and eco-friendly synthesis of indolyl-pyrazolo-pyrimidine derivatives 4a-c by using conventional method via one-pot multi-component reaction has been described. The structures of all these unknown compounds have been confirmed with the help of physical and spectroscopic techniques like IR, 1H and 13C NMR and mass spectrometry and these newly synthesized compounds have been evaluated for in vitro antimicrobial and antitubercular and antioxidant activities. The results reveal that compound 4a exhibits promising antimicrobial, antitubercular and antioxidant properties when compared to the standard drugs.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.61(10) [Oct 2022]en_US
dc.subjectIndoleen_US
dc.subjectPyrazoleen_US
dc.subjectPyrimidin-2-oneen_US
dc.subjectAntimicrobial activityen_US
dc.subjectAntitubercular activityen_US
dc.titleDesign of an efficient three component one-pot synthesis of -1,2,3,4-tetrahydro-4-oxo-6-(5-substituted 2-phenyl-1H-indol-3-yl)-2-thioxopyrimidine-5-carbonitrile as antimicrobial and antitubercular agenten_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i10.67200en_US
Appears in Collections:IJC Vol.61(10) [Oct 2022]

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