Synthesis of 4-octyl-2H-1,4-benzo-thiazin-3-ones.

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dc.contributor.authorGuarda, Vera Lúcia de Miranda
dc.contributor.authorPerrissin, Monique
dc.contributor.authorThomasson, François
dc.contributor.authorXimenes, Eulália Camelo Pessoa de Azevedo
dc.contributor.authorGaldino, Suely Lins
dc.contributor.authorPitta, Ivan da Rocha
dc.contributor.authorLuu-Duc, Cuong
dc.contributor.authorBarbe, Jacques
dc.date.accessioned2017-10-11T16:32:42Z
dc.date.available2017-10-11T16:32:42Z
dc.date.issued2003
dc.description.abstractSynthesis, physical and analytical properties of 6-alkylacylamino-4-octyl-2H-1,4-benzo-thiazin-3-ones derivatives are described. These new compounds were prepared by acylation and/or alkylation of the amino group under phase transfer catalysis conditions. Acid hydrolysis of the alkylacylamino-2H-1,4-benzo-thiazin-3-ones afforded N-alkylamino-benzothiazin-3-ones. Some of these compounds were evaluated in vitro for possible bacteriostatic activity.pt_BR
dc.identifier.citationGUARDA, V. L. de M. et al. Synthesis of 4-octyl-2H-1,4-benzo-thiazin-3-ones. European Journal of Medicinal Chemistry, Paris, v. 38, p. 769-793, 2003. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0223523403001272>. Aesso em: 20 jan. 2017.pt_BR
dc.identifier.doihttps://doi.org/10.1016/S0223-5234(03)00127-2
dc.identifier.issn0223-5234
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/8935
dc.identifier.uri2http://www.sciencedirect.com/science/article/pii/S0223523403001272pt_BR
dc.language.isoen_USpt_BR
dc.rightsrestritopt_BR
dc.subject1,4-Benzothiazinespt_BR
dc.subjectAntibacterialspt_BR
dc.titleSynthesis of 4-octyl-2H-1,4-benzo-thiazin-3-ones.pt_BR
dc.typeArtigo publicado em periodicopt_BR
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