Please use this identifier to cite or link to this item: http://repositorio.ufc.br/handle/riufc/9938
Type: Artigo de Periódico
Title: A convenient synthesis and cytotoxic activity of 3-aryl-5-pentyl-1,2,4-oxadiazoles from carboxylic acid esters and arylamidoximes under solvent-free conditions
Authors: Barros, Carlos Jonnatan Pimentel
Souza, Zilyane Cardoso de
Freitas, Jucleiton José Rufino de
Silva, Paulo Bruno Norberto da
Militão, Gardenia Carmen Gadelha
Silva, Teresinha Gonçalves da
Freitas, Juliano Carlo Rufino
Freitas Filho, João Rufino de
Keywords: Ésteres;Frutas
Issue Date: Mar-2014
Publisher: Journal of the Chilean Chemical Society
Citation: BARROS, 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.
Abstract: The 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.
URI: http://www.repositorio.ufc.br/handle/riufc/9938
ISSN: 0717-9707
Appears in Collections:DFIFA - Artigos publicados em revista científica

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