Green synthesis, antioxidant and antibacterial activities of 4-aryl-3,4- dihydropyrimidinones/thiones derivatives of curcumin. Theoretical calculations and mechanism study

dc.contributor.authorKhaldi-Khellafi, Nassima
dc.contributor.authorMakhloufi-Chebli, Malika
dc.contributor.authorOukacha-Hikem, Djamila
dc.contributor.authorTerachet Bouaziz, Souhila
dc.contributor.authorOuld Lamara, Kamilia
dc.contributor.authorIdir, Taous
dc.contributor.authorBenazzouz-Touami, Amina
dc.contributor.authorDumas, Françoise
dc.date.accessioned2025-10-07T09:52:00Z
dc.date.issued2019
dc.description.abstract3,4-Dihydropyrimidin-2(1H)-one/thione analogs of curcumin were synthesized in good yield by a onepot multi-component cyclocondensation using curcumin, substituted aromatic aldehydes, and urea/ thiourea in less volume of ethanol catalysed by commercial heteropolyacide Keggin type H3PMo12O40 5% mol as a recyclable and nontoxic catalyst under conventional heating and microwave irradiation. All the synthesized curcumin derivatives 4aen were screened for antioxidant and antimicrobial activity. Biological activity data of the synthesized showed that most of the synthesized compounds exhibited greater antioxidant and antibacterial activity than curcumin. Geometries of synthesized compounds were optimized by using B3LYP method with 6-31G* basis set. Then, DFT based reactivity descriptors such as HOMO, LUMO, chemical hardness, electronegativity, chemical potential were calculated and discussed.
dc.identifier.urihttps://dspace.univ-boumerdes.dz/handle/123456789/15536
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofseriesJournal of Molecular Structure/ 1181 (2019) ; pp. 261-269
dc.subjectNitrogen heterocycles
dc.subjectCurcumin-dihydropyrimidinones/thiones
dc.subjectMicrowave irradiation
dc.subjectAntioxidant capacity
dc.subjectAntibacterial activity
dc.subjectTheoretical studies
dc.titleGreen synthesis, antioxidant and antibacterial activities of 4-aryl-3,4- dihydropyrimidinones/thiones derivatives of curcumin. Theoretical calculations and mechanism study
dc.typeArticle

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