Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/697
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dc.contributor.authorKakadiya, Sandip P.-
dc.contributor.authorPurohit, Heta D.-
dc.contributor.authorPurohit, Dipak M.-
dc.date.accessioned2021-08-18T10:47:56Z-
dc.date.available2021-08-18T10:47:56Z-
dc.date.issued2017-08-09-
dc.identifier.citationKakadiya, S. P., Purohit, H. D., & Purohit, D. M. (2014). SYNTHESIS AND BIOLOGICAL SCREENING OF (E)-3-{[(3′-DIFLUOROMETHOXY)-5′-(3 ″-METHYL)-4 ″-(2‴, 2‴, 2‴-TRIFLUOROETHOXY) PYRIDIN-2 ″-YL] METHOXYPHENYL}-1-ARYL-PROP-2-ENE-1-ONES. World Journal of Pharmaceutical Research, 6(11), 888-894.en_US
dc.identifier.issn2277– 7105-
dc.identifier.urihttps://www.wjpr.net/abstract_show/7951-
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/697-
dc.description.abstractChalcones are intermediate compounds to synthesis of many heterocyclic compounds. They are especially interesting for their biological and industrial application. (E)-3-{[(3′-Difluoromethoxy)-5′-(3″-methyl)-4″-(2‴,2‴,2‴-trifluoroethoxy) pyridine-2″-yl]methoxyphenyl}-1-aryl-prop-2-ene-1-ones (4a-4k) have been synthesized by the condensation of 3-Difluoromethoxy-4-{[(3′-methyl)- 4′-(2″,2″,2″-trifluoro ethoxy)pyridin-2′-yl]methoxyphenyl}-1- carboxaldehyde with aromatic ketones in presence of aqueous NaOH. All synthesized compounds characterized with IR, 1H NMR, Mass spectra, TLC and physical constants. All the synthesized compounds evaluated for their antimicrobial activity against Gram +ve bacteria (B.mega, B.Subtillis) Gram -ve bacteria (E.coli, P.fluorescens) and fungi (A.awamori).en_US
dc.language.isoen_USen_US
dc.publisherWorld Journal of Pharmaceutical Researchen_US
dc.subjectChalcones, Anti-microbial activity; (Heterocyclic Compounds).en_US
dc.titleSynthesis And Biological Screening Of (E)-3-{[(3′- Difluoromethoxy)-5′-(3″-Methyl)-4″-(2‴, 2‴, 2‴- Trifluoroethoxy)Pyridin-2″-Yl]Methoxyphenyl}-1- Aryl-Prop-2-Ene-1-Onesen_US
dc.typeArticleen_US
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