Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/66200
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dc.contributor.authorJ Solanki, Manish-
dc.contributor.authorR Vaccharajani, P-
dc.contributor.authorB Audichya, Vipul-
dc.date.accessioned2025-07-24T09:28:15Z-
dc.date.available2025-07-24T09:28:15Z-
dc.date.issued2025-07-
dc.identifier.issn2583-1321 (Online);0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/66200-
dc.description657-662en_US
dc.description.abstractPyrimidine and its derivatives play a significant role in bioactive heterocyclic compounds especially for antibacterial and as well as antifungal activities. By keeping these as central facts, some newly designed pyrimidine derivatives of 5-[N- (substitutedphenyl)]-carboxamido-1,2,3,6-tetrahydro-1,4-dimethyl-2-oxo-6-(m-phenoxyphenyl)-pyrimidines 4a-j have been synthesized by the condensation of m-phenoxybenzaldehyade, N-(4-substitutedphenyl)-oxobutanamides and N-methyl urea in presence of catalytic amount of acid. The structure of these synthesized novel compounds have been confirmed by methods like IR, NMR and mass spectroscopy, and screened for their antibacterial activities.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.64(07) [July 2025]en_US
dc.subjectm-Phenoxybenzaldehydeen_US
dc.subjectBiginelli reactionen_US
dc.subjectPyrimidinesen_US
dc.subjectSpectral studiesen_US
dc.subjectAntibacterial activityen_US
dc.titleDesign, synthesis, characterization and biological evaluation, of novel N-substituted 1,2,3,4-tetrahydropyrimidines-5-carboxamide derivativesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i7.10478en_US
Appears in Collections:IJC Vol.64(07) [July 2025]

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