1. RI UFLA
  2. Instituto de Ciências Naturais - ICN
  3. Departamento de Química - DQI
  4. DQI - Artigos publicados em periódicos
Please use this identifier to cite or link to this item: http://repositorio.ufla.br/jspui/handle/1/41855
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dc.creatorGuimarães, Luiz Gustavo de Lima-
dc.creatorCardoso, Maria das Graças-
dc.creatorLucas, Esther Maria Ferreira-
dc.creatorFreitas, Matheus Puggina de-
dc.creatorFrancisco, Welington-
dc.creatorNelson, David Lee-
dc.date.accessioned2020-07-12T23:49:46Z-
dc.date.available2020-07-12T23:49:46Z-
dc.date.issued2015-06-
dc.identifier.citationGUIMARÃES, L. G. de L. et al. Structural elucidation of a new sesquiterpene alcohol by comparative NMR Studies. Records of Natural Products, [S.l.], v. 9, n. 2, p. 201-207, 2015.pt_BR
dc.identifier.urihttp://acgpubs.org/article/records-of-natural-products/2015/2-april-june/structural-elucidation-of-a-new-sesquiterpene-alcohol-by-comparative-nmr-studiespt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/41855-
dc.description.abstractThe principal constituent of the essential oil from the leaves of the Cordia verbenacea plants collected in Minas Gerais, Brazil had a GC retention time similar to that of α-bisabolol, a sesquiterpene alcohol with important biological properties. NMR analyses ( 1H, 13C, DEPT-135, COSY, HMQC and HMBC) comparing the purified compound with α-bisabolol compound revealed that the new alcohol is an isomer structural of α-bisabolol, due to change in relation to the position of the double bond and the methyl group present in the cyclic chain of these compounds.pt_BR
dc.languageen_USpt_BR
dc.publisherACG Publicationspt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceRecords of Natural Productspt_BR
dc.subjectSesquiterpene alcoholpt_BR
dc.subjectCordia verbenaceapt_BR
dc.subjectα-bisabololpt_BR
dc.subjectNMRpt_BR
dc.subjectNuclear magnetic resonance (NMR)pt_BR
dc.titleStructural elucidation of a new sesquiterpene alcohol by comparative NMR Studiespt_BR
dc.typeArtigopt_BR
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