Show simple item record

dc.creatorPaul, Dhivya
dc.creatorReddy Gontu, Ramanjaneya
dc.creatorParameswaran Rajendran, Subramanian
dc.date2018-06-25
dc.date.accessioned2019-11-13T15:11:47Z
dc.date.available2019-11-13T15:11:47Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/681
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/112685
dc.descriptionAn efficient and greener synthesis of a series of dihydropyrimidone (DHPMs)/ dihydropyrimithione (DHPMTs) derivatives were accomplished via three component one pot condensation between quinoline aldehyde (2-hydroxy-4-formyl quinoline/2-formyl-4-methoxy quinoline) , β – keto ester (ethyl acetoacetate / methyl acetoacetate) and urea/ thiourea using nickel(II) exchanged zeolite [Ni(II)Y] (NiNPs). The NiNPs were characterized by Infrared spectroscopy, Powder X ray diffraction patterns, Electronic microscopy studies- Scanning Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM). After the course of the reaction, the NiNPs were recovered and reused without any apparent loss of activity. The newly synthesized compounds were screened for antimicrobial activity against two human bacterial pathogens, the Gram-positive Methicillin resistant Staphylococcus aureus (MRSA) and the Gram-negative Pseudomonas aeruginosa (MTCC 201) and a human yeast pathogen, Fluconazole resistant Candida albicans (FRCA). The synthesised compounds were also evaluated for their antioxidant activity and the compounds show significant scavenging activity compared to aspartic acid.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/681/239
dc.rightsCopyright (c) 2018 Journal of the Chilean Chemical Societyen-US
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 63 No 2 (2018): Journal of the Chilean Chemical Societyen-US
dc.source0717-9707
dc.source0717-9324
dc.subjectNickel (II) exchanged zeolite [Ni(II)Y]en-US
dc.subjectBiginelli reactionen-US
dc.subjectmicrowave irradiationen-US
dc.subjectgreen conditionen-US
dc.subjecthuman pathogensen-US
dc.subjectDPPH radical scavenging activityen-US
dc.titleFACILE ECOFRIENDLY ONE POT SYNTHESIS OF HETEROCYCLIC PRIVILEDGED MEDICINAL SCAFFOLDS VIA BIGINELLI REACTION USING RETRIEVABLE NICKEL NANOPARTICLES AS CATALYSTen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


This item appears in the following Collection(s)

Show simple item record