Liliane M. F. Porte
Universidade Federal de Santa Maria
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Liliane M. F. Porte.
Food Chemistry | 2013
Valéria Dal Prá; Carolina Bolssoni Dolwitsch; Géssica Domingos da Silveira; Liliane M. F. Porte; Clarissa P. Frizzo; Marcus V. Tres; Vinícius Mossi; Marcio A. Mazutti; Paulo Cícero do Nascimento; Denise Bohrer; Leandro M. de Carvalho; Carine Viana; Marcelo Barcellos da Rosa
In this work were extracted bioactive compounds from Brassica oleracea var capitata using supercritical CO2 and evaluated the antioxidant potential of the extracts. Five extractions were accomplished to investigate the influence of pressure (10-25 MPa) and temperature (20-60 °C) in the extraction yield, chemical composition and antioxidant potential towards peroxyl, superoxide and hydroxyl radicals. The highest extraction yield was obtained at 60 °C and 25 MPa, which was 0.47 wt% (run 2). In the characterisation of the extracts obtained was possible the identification of sulforaphane and iberin nitrile that present known biological properties. The extracts of all runs presented antioxidant activities towards the three radicals, but the highest activities for all radicals were using the extracts obtained in the run 2. The use of supercritical CO2 extraction to obtain bioactive compounds of B. oleracea var capitata showed to be a promising alternative to conventional extraction methods, since allowed the extraction of compounds with scientific and industrial interest.
Journal of the Brazilian Chemical Society | 2009
Helio G. Bonacorso; Renata P. Vezzosi; Isadora R. Rodrigues; Roberta L. Drekener; Liliane M. F. Porte; Alex F. C. Flores; Nilo Zanatta; Marcos A. P. Martins
Two new trifluoroacetylketene O,N-acetals [CF3C(O)CH=C(OEt)(NS(O)R2), where R = CH3, Ph] derived from the reaction of 4,4-diethoxy-1,1,1-trifluorobut-3-en-2-one [CF3C(O)CH=C(OEt)2] with S,S-dimethyl- and S-methyl-S-phenyl-sulfoximide [HN=S(O)R2], in the presence of triethylamine, have been obtained, in 60-72% yields, and applied in the synthesis of S,S-dimethylsulfoximido-substituted pyrazoles, isoxazoles and pyrimidines, in 55-89% yields, from the reactions of 4-ethoxy-4-(S,S-dimethylsulfoximido)-1,1,1-trifluorobut-3-en-2-one with hydrazines, hydroxylamine hydrochloride and acetylguanidine.
Química Nova | 2012
Thiago Guilherme Schwanz; Susana Mohr; Liliane M. F. Porte; Nilo Zanatta; Helio G. Bonacorso; Marcos A. P. Martins; Joni Hilda Costabeber
This paper describes an analytical method for analyzing polychlorinated biphenyls in corn samples using solid phase extraction (SPE) followed by determination by GC-MS. All calibration curves proved linear (r> 0.99). Recoveries ranged between 74.1 and 110.6% with relative standard deviation lower than 20% for all compounds. The limits of quantitation for the method were between 0.025 and 0.1 ng g-1. Of the 51 samples analyzed, PCB 180 showed the highest frequency, being detected in more than 39%, followed by PCB 138, detected in more than 33% of samples.
Journal of the Brazilian Chemical Society | 2010
Helio G. Bonacorso; Cleber A. Cechinel; Everton P. Pittaluga; Adriana Ferla; Liliane M. F. Porte; Marcos A. P. Martins; Nilo Zanatta
This paper describes the conventional regioselective synthesis of a series of new succinyl spacer bis-(3,5-substituted 2-pyrazolines and 1H-pyrazoles), namely; 1,4-bis[5-(trifluoromethyl)-5-hydroxy-4,5-dihydro-1H-pyrazol-1-yl]butane-1,4-diones (46-88%) and the respective dehydrated system (60-78%), new 1-[5-(trifluoromethyl)-5-hydroxy-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutane hydrazides (52-81%) and the non-symmetrical 2-pyrazolines derivatives thereof as 1-[5-(trifluoromethyl)-5-hydroxy-4,5-dihydro-1H-pyrazol-1-yl)-4-(5-(trichloromethyl)-5-hydroxy-4,5-dihydro-1H-pyrazol-1-yl]butane-1,4-diones (75-91%). All succinyl substituted bispyrazoles were obtained from the cyclocondensation reactions of 4-substituted 4-alkoxy-1,1,1-trihaloalk-3-en-2-ones, where the 4-substituents are H, Me, Ph, 4-FC6H4, 4-ClC6H4, 4-OMeC6H4, 4-NO2C6H4, 1-naphthyl and 2-furyl, with succinic acid dihydrazide in ethanol as solvent under controlled reaction conditions.
Journal of Fluorine Chemistry | 2012
Helio G. Bonacorso; Susiane Cavinatto; Patrick T. Campos; Liliane M. F. Porte; Jussara Navarini; Gisele R. Paim; Marcos A. P. Martins; Nilo Zanatta; Caroline Z. Stüker
Tetrahedron Letters | 2009
Helio G. Bonacorso; Liliane M. F. Porte; Cleber A. Cechinel; Gisele R. Paim; Everton D. Deon; Nilo Zanatta; Marcos A. P. Martins
Tetrahedron Letters | 2012
Helio G. Bonacorso; Michele S. Correa; Liliane M. F. Porte; Everton P. Pittaluga; Nilo Zanatta; Marcos A. P. Martins
Tetrahedron Letters | 2010
Helio G. Bonacorso; Liliane M. F. Porte; Gisele R. Paim; Fábio M. Luz; Marcos A. P. Martins; Nilo Zanatta
Journal of Fluorine Chemistry | 2013
Helio G. Bonacorso; Jussara Navarini; Liliane M. F. Porte; Everton P. Pittaluga; Alexandre R. Meyer; Marcos A. P. Martins; Nilo Zanatta
Journal of Fluorine Chemistry | 2010
Helio G. Bonacorso; Guilherme P. Bortolotto; Jussara Navarini; Liliane M. F. Porte; Carson W. Wiethan; Nilo Zanatta; Marcos A. P. Martins; Alex F. C. Flores