Filtros : "Indexado no EMBASE" "QUÍMICA" Removidos: "ARTIGO DE JORNAL-TRADUCAO" "Manole" "FO-ODP" Limpar

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  • Source: Rapid Communications in Mass Spectrometry. Unidade: FCFRP

    Subjects: ALCALOIDES, FARMACOLOGIA, ANIMAIS, PESOS E MEDIDAS CORPORAIS, RAIZ, PLANTAS, ESPECTROMETRIA DE MASSAS, QUÍMICA

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      GAZOLLA, Matheus Coutinho et al. Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity. Rapid Communications in Mass Spectrometry, v. 34, 2020Tradução . . Disponível em: https://doi.org/10.1002/rcm.8705. Acesso em: 30 ago. 2024.
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      Gazolla, M. C., Marques, L. M. M., Silva, M. G. e, Araújo, M. T. M. F., Mendes, R. L., Almeida, J. R. G. da S., et al. (2020). Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity. Rapid Communications in Mass Spectrometry, 34. doi:10.1002/rcm.8705
    • NLM

      Gazolla MC, Marques LMM, Silva MG e, Araújo MTMF, Mendes RL, Almeida JRG da S, Vessecchi R, Lopes NP. Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity [Internet]. Rapid Communications in Mass Spectrometry. 2020 ; 34[citado 2024 ago. 30 ] Available from: https://doi.org/10.1002/rcm.8705
    • Vancouver

      Gazolla MC, Marques LMM, Silva MG e, Araújo MTMF, Mendes RL, Almeida JRG da S, Vessecchi R, Lopes NP. Characterization of 3‐aminospirostane alkaloids from roots of Solanum paniculatum L. with hepatoprotective activity [Internet]. Rapid Communications in Mass Spectrometry. 2020 ; 34[citado 2024 ago. 30 ] Available from: https://doi.org/10.1002/rcm.8705
  • Source: Journal of Natural Products. Unidade: FCFRP

    Subjects: BACTÉRIAS, QUÍMICA, FÁRMACOS, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)

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      FUKUDA, Taise Tomie Hebihara et al. Research tales from the Clardy Laboratory: function-driven natural product discovery. Journal of Natural Products, v. 83, n. 3, p. 744-755, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jnatprod.9b01086. Acesso em: 30 ago. 2024.
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      Fukuda, T. T. H., Cassilly, C. D., Gerdt, J. P., Henke, M. T., Helfrich, E. J. N., & Mevers, E. (2020). Research tales from the Clardy Laboratory: function-driven natural product discovery. Journal of Natural Products, 83( 3), 744-755. doi:10.1021/acs.jnatprod.9b01086
    • NLM

      Fukuda TTH, Cassilly CD, Gerdt JP, Henke MT, Helfrich EJN, Mevers E. Research tales from the Clardy Laboratory: function-driven natural product discovery [Internet]. Journal of Natural Products. 2020 ; 83( 3): 744-755.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01086
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      Fukuda TTH, Cassilly CD, Gerdt JP, Henke MT, Helfrich EJN, Mevers E. Research tales from the Clardy Laboratory: function-driven natural product discovery [Internet]. Journal of Natural Products. 2020 ; 83( 3): 744-755.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1021/acs.jnatprod.9b01086
  • Source: ACS Synthetic Biology. Unidades: FMRP, FFCLRP

    Subjects: ESCHERICHIA COLI, METABOLISMO, PLASMÍDEOS, GENÉTICA, RIBOSSOMOS, QUÍMICA, BIOLOGIA SINTÉTICA

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      SIQUEIRA, Guilherme Marcelino Viana de e SILVA-ROCHA, Rafael e GUAZZARONI, Maria Eugenia. Turning the screw: engineering extreme pH resistance in escherichia coli through combinatorial synthetic operons. ACS Synthetic Biology, v. 9, n. 6, p. 1254-1262, 2020Tradução . . Disponível em: https://doi.org/10.1021/acssynbio.0c00089. Acesso em: 30 ago. 2024.
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      Siqueira, G. M. V. de, Silva-Rocha, R., & Guazzaroni, M. E. (2020). Turning the screw: engineering extreme pH resistance in escherichia coli through combinatorial synthetic operons. ACS Synthetic Biology, 9( 6), 1254-1262. doi:10.1021/acssynbio.0c00089
    • NLM

      Siqueira GMV de, Silva-Rocha R, Guazzaroni ME. Turning the screw: engineering extreme pH resistance in escherichia coli through combinatorial synthetic operons [Internet]. ACS Synthetic Biology. 2020 ; 9( 6): 1254-1262.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1021/acssynbio.0c00089
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      Siqueira GMV de, Silva-Rocha R, Guazzaroni ME. Turning the screw: engineering extreme pH resistance in escherichia coli through combinatorial synthetic operons [Internet]. ACS Synthetic Biology. 2020 ; 9( 6): 1254-1262.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1021/acssynbio.0c00089
  • Source: Journal of Computer-Aided Molecular Design. Unidade: FFCLRP

    Subjects: COLESTEROL, QUÍMICA, TERMODINÂMICA, ELETROSTÁTICA

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      SIANI, Paulo et al. Parameterization of a coarse-grained model of cholesterol with point-dipole electrostatics. Journal of Computer-Aided Molecular Design, v. 32, n. 11, p. 1259-1271, 2018Tradução . . Disponível em: https://doi.org/10.1007/s10822-018-0164-4. Acesso em: 30 ago. 2024.
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      Siani, P., Khandelia, H., Orsi, M., & Dias, L. G. (2018). Parameterization of a coarse-grained model of cholesterol with point-dipole electrostatics. Journal of Computer-Aided Molecular Design, 32( 11), 1259-1271. doi:10.1007/s10822-018-0164-4
    • NLM

      Siani P, Khandelia H, Orsi M, Dias LG. Parameterization of a coarse-grained model of cholesterol with point-dipole electrostatics [Internet]. Journal of Computer-Aided Molecular Design. 2018 ; 32( 11): 1259-1271.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10822-018-0164-4
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      Siani P, Khandelia H, Orsi M, Dias LG. Parameterization of a coarse-grained model of cholesterol with point-dipole electrostatics [Internet]. Journal of Computer-Aided Molecular Design. 2018 ; 32( 11): 1259-1271.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10822-018-0164-4
  • Source: PLOS Computational Biology. Unidade: FCFRP

    Subjects: FORMIGAS, BIOINFORMÁTICA, FUNGOS, QUÍMICA, SIMULAÇÃO, ESPECTROSCOPIA DE MASSA

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      SILVA, Ricardo R. da et al. Propagating annotations of molecular networks using in silico fragmentation. PLOS Computational Biology, v. 14, n. 4, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pcbi.1006089. Acesso em: 30 ago. 2024.
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      Silva, R. R. da, Wang, M., Nothias, L. -F., van der Hooft, J. J. J., Caraballo-Rodríguez, A. M., Fox, E., et al. (2018). Propagating annotations of molecular networks using in silico fragmentation. PLOS Computational Biology, 14( 4). doi:10.1371/journal.pcbi.1006089
    • NLM

      Silva RR da, Wang M, Nothias L-F, van der Hooft JJJ, Caraballo-Rodríguez AM, Fox E, Balunas MJ, Klassen JL, Lopes NP, Dorrestein PC. Propagating annotations of molecular networks using in silico fragmentation [Internet]. PLOS Computational Biology. 2018 ; 14( 4):[citado 2024 ago. 30 ] Available from: https://doi.org/10.1371/journal.pcbi.1006089
    • Vancouver

      Silva RR da, Wang M, Nothias L-F, van der Hooft JJJ, Caraballo-Rodríguez AM, Fox E, Balunas MJ, Klassen JL, Lopes NP, Dorrestein PC. Propagating annotations of molecular networks using in silico fragmentation [Internet]. PLOS Computational Biology. 2018 ; 14( 4):[citado 2024 ago. 30 ] Available from: https://doi.org/10.1371/journal.pcbi.1006089
  • Source: Organic & Biomolecular Chemistry. Unidades: FCFRP, FFCLRP

    Subjects: SESQUITERPENOS, QUÍMICA

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      SASS, Daiane Cristina et al. Selectivity in reduction of natural furanoheliangolides with Stryker's reagent. Organic & Biomolecular Chemistry, v. 9, n. 17, p. 6148-6153, 2011Tradução . . Disponível em: https://doi.org/10.1039/c1ob05734k. Acesso em: 30 ago. 2024.
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      Sass, D. C., Heleno, V. C. G., Morais, G. O., Lopes, J. L. C., Lopes, N. P., & Constantino, M. G. (2011). Selectivity in reduction of natural furanoheliangolides with Stryker's reagent. Organic & Biomolecular Chemistry, 9( 17), 6148-6153. doi:10.1039/c1ob05734k
    • NLM

      Sass DC, Heleno VCG, Morais GO, Lopes JLC, Lopes NP, Constantino MG. Selectivity in reduction of natural furanoheliangolides with Stryker's reagent [Internet]. Organic & Biomolecular Chemistry. 2011 ; 9( 17): 6148-6153.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1039/c1ob05734k
    • Vancouver

      Sass DC, Heleno VCG, Morais GO, Lopes JLC, Lopes NP, Constantino MG. Selectivity in reduction of natural furanoheliangolides with Stryker's reagent [Internet]. Organic & Biomolecular Chemistry. 2011 ; 9( 17): 6148-6153.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1039/c1ob05734k
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      SASS, Daiane Cristina et al. Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, v. 52, n. 41, p. 5371-5374, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.08.039. Acesso em: 30 ago. 2024.
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      Sass, D. C., Lucca Júnior, E. C. de, Barbosa, J. da S., Oliveira, K. T. de, & Constantino, M. G. (2011). Tandem reduction + cyclization of ortho-substituted cinnamic esters. Tetrahedron Letters, 52( 41), 5371-5374. doi:10.1016/j.tetlet.2011.08.039
    • NLM

      Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
    • Vancouver

      Sass DC, Lucca Júnior EC de, Barbosa J da S, Oliveira KT de, Constantino MG. Tandem reduction + cyclization of ortho-substituted cinnamic esters [Internet]. Tetrahedron Letters. 2011 ; 52( 41): 5371-5374.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.tetlet.2011.08.039
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: QUÍMICA

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      NAZARIO, Carlos E. D. et al. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, v. 52, n. 32, p. 4177-4181, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.06.004. Acesso em: 30 ago. 2024.
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      Nazario, C. E. D., Santana, A. S., Kawasoko, C. Y., Carollo, C. A., Hurtado, G. R., Viana, L. H., et al. (2011). Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator. Tetrahedron Letters, 52( 32), 4177-4181. doi:10.1016/j.tetlet.2011.06.004
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      Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
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      Nazario CED, Santana AS, Kawasoko CY, Carollo CA, Hurtado GR, Viana LH, Barbosa SL, Guerrero Junior PG, Marques FA, Dabdoub VB, Dabdoub MJ, Baroni ACM. Synthesis of (Z)-tributylstannyl enynes: systematic studies of Sonogashira cross-coupling reactions between (E)-1-iodovinyl-1-tributylstannanes and terminal acetylenes using amines or tetrabutylammonium hydroxide (TBAOH) as activator [Internet]. Tetrahedron Letters. 2011 ; 52( 32): 4177-4181.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.tetlet.2011.06.004
  • Source: Analytica Chimica Acta. Unidade: IQ

    Subjects: QUÍMICA, PLANEJAMENTO E ANÁLISE DE EXPERIMENTOS

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      BORTOLOTI, João Alexandre e BORGES, Cleber N. e BRUNS, Roy Edward. Split-plot designs and normal probability graphs for the optimization of chemical systems. Analytica Chimica Acta, v. 544, n. 1-2, p. 206-212, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.aca.2005.01.021. Acesso em: 30 ago. 2024.
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      Bortoloti, J. A., Borges, C. N., & Bruns, R. E. (2005). Split-plot designs and normal probability graphs for the optimization of chemical systems. Analytica Chimica Acta, 544( 1-2), 206-212. doi:10.1016/j.aca.2005.01.021
    • NLM

      Bortoloti JA, Borges CN, Bruns RE. Split-plot designs and normal probability graphs for the optimization of chemical systems [Internet]. Analytica Chimica Acta. 2005 ; 544( 1-2): 206-212.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.aca.2005.01.021
    • Vancouver

      Bortoloti JA, Borges CN, Bruns RE. Split-plot designs and normal probability graphs for the optimization of chemical systems [Internet]. Analytica Chimica Acta. 2005 ; 544( 1-2): 206-212.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.aca.2005.01.021
  • Source: Chemometrics and Intelligent Laboratory Systems. Unidade: IQ

    Subjects: VOLTAMETRIA, QUÍMICA, QUIMIOMETRIA

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      BORTOLOTI, João Alexandre et al. Split-plot design optimization for trace determination of lead by anodic stripping voltammetry in a homogeneous ternary solvent system. Chemometrics and Intelligent Laboratory Systems, v. 70, n. 2, p. 113-121, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.chemolab.2003.09.004. Acesso em: 30 ago. 2024.
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      Bortoloti, J. A., Bruns, R. E., Andrade, J. C. de, & Vieira , R. K. (2004). Split-plot design optimization for trace determination of lead by anodic stripping voltammetry in a homogeneous ternary solvent system. Chemometrics and Intelligent Laboratory Systems, 70( 2), 113-121. doi:10.1016/j.chemolab.2003.09.004
    • NLM

      Bortoloti JA, Bruns RE, Andrade JC de, Vieira RK. Split-plot design optimization for trace determination of lead by anodic stripping voltammetry in a homogeneous ternary solvent system [Internet]. Chemometrics and Intelligent Laboratory Systems. 2004 ; 70( 2): 113-121.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.chemolab.2003.09.004
    • Vancouver

      Bortoloti JA, Bruns RE, Andrade JC de, Vieira RK. Split-plot design optimization for trace determination of lead by anodic stripping voltammetry in a homogeneous ternary solvent system [Internet]. Chemometrics and Intelligent Laboratory Systems. 2004 ; 70( 2): 113-121.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.chemolab.2003.09.004
  • Source: Analytica Chimica Acta. Unidade: IQ

    Subjects: AMPEROMETRIA, QUÍMICA

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      FREIRE, Renato Sanches et al. Dual amperometric biosensor device for analysis of binary mixtures of phenols by multivariate calibration using partial least squares. Analytica Chimica Acta, v. 485, n. 2, p. 263-269, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0003-2670(03)00414-8. Acesso em: 30 ago. 2024.
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      Freire, R. S., Ferreira, M. M. C., Durán, N., & Kubota, L. T. (2003). Dual amperometric biosensor device for analysis of binary mixtures of phenols by multivariate calibration using partial least squares. Analytica Chimica Acta, 485( 2), 263-269. doi:10.1016/s0003-2670(03)00414-8
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      Freire RS, Ferreira MMC, Durán N, Kubota LT. Dual amperometric biosensor device for analysis of binary mixtures of phenols by multivariate calibration using partial least squares [Internet]. Analytica Chimica Acta. 2003 ; 485( 2): 263-269.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/s0003-2670(03)00414-8
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      Freire RS, Ferreira MMC, Durán N, Kubota LT. Dual amperometric biosensor device for analysis of binary mixtures of phenols by multivariate calibration using partial least squares [Internet]. Analytica Chimica Acta. 2003 ; 485( 2): 263-269.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/s0003-2670(03)00414-8
  • Source: Analytica Chimica Acta. Unidade: IQ

    Subjects: ESPECTROFOTOMETRIA, FERRO, QUÍMICA

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      SILVA, Marcelo S. Pinto e MASINI, Jorge Cesar. Exploiting monosegmented flow analysis to perform in-line standart additions using a single stock standard solution in spectrophotometric sequential injection procedures. Analytica Chimica Acta, v. 466, n. 2, p. 345-352, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0003-2670(02)00594-9. Acesso em: 30 ago. 2024.
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      Silva, M. S. P., & Masini, J. C. (2002). Exploiting monosegmented flow analysis to perform in-line standart additions using a single stock standard solution in spectrophotometric sequential injection procedures. Analytica Chimica Acta, 466( 2), 345-352. doi:10.1016/s0003-2670(02)00594-9
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      Silva MSP, Masini JC. Exploiting monosegmented flow analysis to perform in-line standart additions using a single stock standard solution in spectrophotometric sequential injection procedures [Internet]. Analytica Chimica Acta. 2002 ; 466( 2): 345-352.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/s0003-2670(02)00594-9
    • Vancouver

      Silva MSP, Masini JC. Exploiting monosegmented flow analysis to perform in-line standart additions using a single stock standard solution in spectrophotometric sequential injection procedures [Internet]. Analytica Chimica Acta. 2002 ; 466( 2): 345-352.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/s0003-2670(02)00594-9

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