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  8. Issue 04
Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/19845
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dc.contributor.authorAhsan Sharif-
dc.contributor.authorEjaz Ahmad-
dc.contributor.authorMunawar Ali Munawar-
dc.contributor.authorShamsa Jabeen-
dc.contributor.authorMisbah-ul-Ain, Khan-
dc.contributor.authorRobina Begum-
dc.contributor.authorAleeza Farrukh-
dc.contributor.authorMuhammad Ashraf-
dc.contributor.authorShafia Arshad-
dc.contributor.authorNighat Afza-
dc.date.accessioned2023-10-17T04:43:57Z-
dc.date.available2023-10-17T04:43:57Z-
dc.date.issued2011-08-20-
dc.identifier.citationSharif, A., Ahmed, E., Munawar, M. A., Jabeen, S., Khan, M. U. A., Begum, R., ... & Afza, N. (2011). Facile syntheses of bioactive 5-arylidenethiobarbituric acids. Journal of the chemical Society of Pakistan, 33(4), 578-586.en_US
dc.identifier.issn0253-5106-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/19845-
dc.description.abstractA simple and green chemistry route for the preparation of 5- arylidenethiobarbituric acids has been developed by Knoevenagel condensation of thiobarbituric acid with different aromatic and heteroaromatic aldehydes using catalytic amount of acetic acid by grinding in mortar and pestle. The title compounds were obtained in good to high yields (50-89%) and characterized by IR, NMR, mass spectroscopy and elemental analysis. All compounds exhibited DPPH radical scavenging and antibacterial activities, respectively.en_US
dc.description.sponsorshipThe chemical society of Pakistan is an approved society from the PSF.en_US
dc.language.isoenen_US
dc.publisherHEJ Research Institute of Chemistry, University of Karachi, Karachi.en_US
dc.titleFACILE SYNTHESES OF BIOACTIVE 5-ARYLIDENETHIOBARBITURIC ACIDSen_US
dc.typeArticleen_US
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