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dc.contributor.authorBarros, Carlos Jonnatan Pimentel-
dc.contributor.authorSouza, Zilyane Cardoso de-
dc.contributor.authorFreitas, Jucleiton José Rufino de-
dc.contributor.authorSilva, Paulo Bruno Norberto da-
dc.contributor.authorMilitão, Gardenia Carmen Gadelha-
dc.contributor.authorSilva, Teresinha Gonçalves da-
dc.contributor.authorFreitas, Juliano Carlo Rufino-
dc.contributor.authorFreitas Filho, João Rufino de-
dc.date.accessioned2014-11-26T11:51:32Z-
dc.date.available2014-11-26T11:51:32Z-
dc.date.issued2014-03-
dc.identifier.citationBARROS, C. J. P. et al. A convenient synthesis and cytotoxic activity of 3-aryl-5-pentyl-1,2,4-oxadiazoles from carboxylic acid esters and arylamidoximes under solvent-free onditions. Journal of the Chilean Chemical Society, Concepcíon, v. 59, n. 1, p. 2359-2362, mar. 2014.pt_BR
dc.identifier.issn0717-9707-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/9938-
dc.description.abstractThe synthesis of 3-aryl-5-pentyl-1,2,4-oxadiazoles from carboxylic acid esters and arylamidoximes in the presence of potassium carbonate is described. The reaction was carried out in a microwave oven without any solvent in much shorter time and in good yields. The structures of the synthesized compounds were elucidated using IR, 1H and 13C NMR spectroscopy and elemental analysis and their antiproliferative activities was evaluated against three different human cell lines.pt_BR
dc.language.isoenpt_BR
dc.publisherJournal of the Chilean Chemical Societypt_BR
dc.subjectÉsterespt_BR
dc.subjectFrutaspt_BR
dc.titleA convenient synthesis and cytotoxic activity of 3-aryl-5-pentyl-1,2,4-oxadiazoles from carboxylic acid esters and arylamidoximes under solvent-free conditionspt_BR
dc.typeArtigo de Periódicopt_BR
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