DEFAR - Departamento de Farmácia
URI permanente desta comunidadehttp://www.hml.repositorio.ufop.br/handle/123456789/530
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Resultados da Pesquisa
Item Selective oxidation of lupeol by iodosylbenzene catalyzed by manganese porphyrins.(2016) Martins, Dayse Carvalho da Silva; Silva, Fernando César; Meireles, Alexandre Moreira; Soares, Érico Augusto Rodrigues; Silva, Grácia Divina de Fátima; Vieira Filho, Sidney Augusto; Duarte, Lucienir Pains; Rebouças, Júlio Santos; Idemori, Ynara MarinaManganese porphyrin-catalyzed oxidation of lupeol by iodosylbenzenewas achieved undermild conditionswith low isolated yields but with remarkable selectivity, depending on the catalyst of choice. Mn(III) mesotetraphenylporphyrin and Mn(III) meso-tetrakis(4-carbomethoxyphenyl)porphyrin provided an entry for the preparation of 3β,30-dihydroxylup-20(29)-ene (6–14% yields), whereas Mn(III) β-octabromo-meso-tetrakis(4- carbomethoxyphenyl)porphyrin led to 20-oxo-3β-hydroxy-29-norlupeol (6% yield), as single products. Unreacted lupeol was recovered in quantitative yield. The oxidative transformations at lupeol C20 or C30 take place with no need for protection of C3 hydroxyl moiety.Item Total assignment of 1H and 13C NMR spectra of two 3,4-secofriedelanes from Austroplenckia populnea.(2001) Vieira Filho, Sidney Augusto; Duarte, Lucienir Pains; Silva, Grácia Divina de Fátima; Lula, Ivana Silva; Santos, Marcelo Henrique dosTwo new 3,4-secofriedelanes, 3,4-seco-28-hydroxyfriedelan-3-oic acid (1) and 3,4-secofriedelan-3-oic acid (2),were isolated from the leaves of Austroplenckia populnea (Celastraceae).The structureswere established by 2D NMR spectroscopic techniques (COSY, HMQC, HMBC and NOESY).Item Epikatonic acid from Austroplenckia populnea : structure elucidation by nmr spectroscopy and x-ray crystallography.(2002) Silva, Grácia Divina de Fátima; Duarte, Lucienir Pains; Viera Filho, Sidney Augusto; Doriguetto, Antônio Carlos; Mascarenhas, Yvone PrimeranoFrom the chloroform extract of Austroplenckia populnea, epikatonic acid, friedelin, populnonic acid, abruslactone A, salaspermic acid and 22b-epi-maytenfolic acid were isolated. The structure and stereochemistry of epikatonic acid were established by two-dimensional NMR spectroscopic techniques (HMQC, HMBC and NOESY) and later confirmed by single crystal X-ray diffraction as 3b-hydroxyolean- 12-en-29-oic acid, which unambiguously established the configuration of the hydroxyl group at C-3 as 3b-OH and the carboxyl group at C-20 as 20a-COOH. The crystal structure shows two independent molecules in the asymmetric unit. The crystal packing is stabilized by four O–H· · ·O intermolecular hydrogen bonds, which give rise to infinite double chains along the c axis.