Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60725
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dc.contributor.authorMarri, Srinivas-
dc.date.accessioned2022-10-21T05:57:27Z-
dc.date.available2022-10-21T05:57:27Z-
dc.date.issued2022-10-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60725-
dc.description1046-1053en_US
dc.description.abstractSynthesis of novel 5-methyl-1-(4-(6-methylimidazo[1,2-b]isoxazol-3-yl)phenyl)-3-aryl-1,3,5-triazinane-2-thiones 6 has been achieved by the reaction of 3-amino-5-methylisoxazole 1 with p-nitrophenacyl bromide, followed by reduction of 3 with stannous chloride. Compounds 4 on treatment with different aryl isothiocyanates in refluxing benzene, followed by trimolecular condensation with 30% HCHO and methyl amine in ethanol affords the title compounds 6. The newly synthesized compounds 6 have been evaluated for their in vitro antimicrobial activity. Compounds 6 exhibit potent antimicrobial activity compared to that of standard drugs.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.61(10) [Oct 2022]en_US
dc.subject6-Methyl-3-arylimidazolo[1,2-b]isoxazolesen_US
dc.subject1,3,5-Triazinane-2-thionesen_US
dc.subjectTrimolecular condensationen_US
dc.subjectAntibacterial activityen_US
dc.subjectAntifungal activityen_US
dc.titleSynthesis and antimicrobial activity of novel 5-methyl-1-(4-(6-methylimidazo [1,2-b]isoxazol-3-yl)phenyl)-3-aryl-1,3,5-triazinane-2-thionesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i10.62377en_US
Appears in Collections:IJC Vol.61(10) [Oct 2022]

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