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  • Source: RSC Advances. Unidades: IQSC, IQ

    Subjects: ENZIMAS, CATÁLISE

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    • ABNT

      FERREIRA , Irlon Maciel et al. Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins. RSC Advances, v. 7, p. 12650-12658, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7ra00083a. Acesso em: 06 out. 2024.
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      Ferreira , I. M., Yoshioka, S. A., Comasseto, J. V., & Porto, A. L. M. (2017). Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins. RSC Advances, 7, 12650-12658. doi:10.1039/c7ra00083a
    • NLM

      Ferreira IM, Yoshioka SA, Comasseto JV, Porto ALM. Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins [Internet]. RSC Advances. 2017 ; 7 12650-12658.[citado 2024 out. 06 ] Available from: https://doi.org/10.1039/c7ra00083a
    • Vancouver

      Ferreira IM, Yoshioka SA, Comasseto JV, Porto ALM. Immobilization of amano lipase from pseudomonas fluorescens on silk fibroin spheres: an alternative protocol for the enantioselective synthesis of halohydrins [Internet]. RSC Advances. 2017 ; 7 12650-12658.[citado 2024 out. 06 ] Available from: https://doi.org/10.1039/c7ra00083a
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: QUÍMICA, CÉLULAS

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      PIOVAN, Leandro et al. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms. Tetrahedron - Asymmetry, v. 19, n. 20, p. 2385-2389, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.10.003. Acesso em: 06 out. 2024.
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      Piovan, L., Kagohara, E., Ricci, L. C., Keppler, A. F., Capelari, M., Andrade, L. H., et al. (2008). Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms. Tetrahedron - Asymmetry, 19( 20), 2385-2389. doi:10.1016/j.tetasy.2008.10.003
    • NLM

      Piovan L, Kagohara E, Ricci LC, Keppler AF, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms [Internet]. Tetrahedron - Asymmetry. 2008 ; 19( 20): 2385-2389.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2008.10.003
    • Vancouver

      Piovan L, Kagohara E, Ricci LC, Keppler AF, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms [Internet]. Tetrahedron - Asymmetry. 2008 ; 19( 20): 2385-2389.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2008.10.003
  • Source: Talanta. Unidades: IQ, IQSC

    Subjects: ELETROQUÍMICA, VOLTAMETRIA

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      CESARINO, Ivana et al. Evaluation of a carbon paste electrode modified with organofunctionalised SBA-15 nanostructured silica in the simultaneous determination of divalent lead, copper and mercury ions. Talanta, v. 75, n. 1, p. 15-21, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.talanta.2007.06.032. Acesso em: 06 out. 2024.
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      Cesarino, I., Marino, G., Matos, J. do R., & Cavalheiro, E. T. G. (2008). Evaluation of a carbon paste electrode modified with organofunctionalised SBA-15 nanostructured silica in the simultaneous determination of divalent lead, copper and mercury ions. Talanta, 75( 1), 15-21. doi:10.1016/j.talanta.2007.06.032
    • NLM

      Cesarino I, Marino G, Matos J do R, Cavalheiro ETG. Evaluation of a carbon paste electrode modified with organofunctionalised SBA-15 nanostructured silica in the simultaneous determination of divalent lead, copper and mercury ions [Internet]. Talanta. 2008 ; 75( 1): 15-21.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.talanta.2007.06.032
    • Vancouver

      Cesarino I, Marino G, Matos J do R, Cavalheiro ETG. Evaluation of a carbon paste electrode modified with organofunctionalised SBA-15 nanostructured silica in the simultaneous determination of divalent lead, copper and mercury ions [Internet]. Talanta. 2008 ; 75( 1): 15-21.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.talanta.2007.06.032
  • Source: Enzyme and Microbial Technology. Unidades: ICB, IQ, IQSC

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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      RAMINELLI, Cristiano et al. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, v. 40, n. 2, p. 362-369, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2006.06.002. Acesso em: 06 out. 2024.
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      Raminelli, C., Kagohara, E., Pellizari, V. H., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2007). Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, 40( 2), 362-369. doi:10.1016/j.enzmictec.2006.06.002
    • NLM

      Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
    • Vancouver

      Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, SÍNTESE ORGÂNICA, ASPERGILLUS

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      OMORI, Álvaro Takeo et al. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1048-1053, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.04.019. Acesso em: 06 out. 2024.
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      Omori, Á. T., Assis, L. F., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, 18( 9), 1048-1053. doi:10.1016/j.tetasy.2007.04.019
    • NLM

      Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
    • Vancouver

      Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: Photochemistry and Photobiology. Unidades: IQ, IQSC

    Assunto: BIOQUÍMICA

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      OLIVEIRA, Marilene Silva et al. Quenching of singlet molecular oxygen,'O.IND.2'('ANTIPOT.1 DELTA IND.G), by dipyridamole and derivatives. Photochemistry and Photobiology, v. 83, n. 6, p. 1379-1385, 2007Tradução . . Disponível em: http://www.blackwell-synergy.com/doi/pdf/10.1111/j.1751-1097.2007.00174.x. Acesso em: 06 out. 2024.
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      Oliveira, M. S., Lima, M., Severino, D., Baptista, M. da S., Di Mascio, P., & Tabak, M. (2007). Quenching of singlet molecular oxygen,'O.IND.2'('ANTIPOT.1 DELTA IND.G), by dipyridamole and derivatives. Photochemistry and Photobiology, 83( 6), 1379-1385. Recuperado de http://www.blackwell-synergy.com/doi/pdf/10.1111/j.1751-1097.2007.00174.x
    • NLM

      Oliveira MS, Lima M, Severino D, Baptista M da S, Di Mascio P, Tabak M. Quenching of singlet molecular oxygen,'O.IND.2'('ANTIPOT.1 DELTA IND.G), by dipyridamole and derivatives [Internet]. Photochemistry and Photobiology. 2007 ; 83( 6): 1379-1385.[citado 2024 out. 06 ] Available from: http://www.blackwell-synergy.com/doi/pdf/10.1111/j.1751-1097.2007.00174.x
    • Vancouver

      Oliveira MS, Lima M, Severino D, Baptista M da S, Di Mascio P, Tabak M. Quenching of singlet molecular oxygen,'O.IND.2'('ANTIPOT.1 DELTA IND.G), by dipyridamole and derivatives [Internet]. Photochemistry and Photobiology. 2007 ; 83( 6): 1379-1385.[citado 2024 out. 06 ] Available from: http://www.blackwell-synergy.com/doi/pdf/10.1111/j.1751-1097.2007.00174.x
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, HIDROGENAÇÃO, LIPASE

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      FERRAZ, Helena Maria Carvalho et al. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1070-1076, 2007Tradução . . Acesso em: 06 out. 2024.
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      Ferraz, H. M. C., Bianco, G. G., Teixeira, C. C., Andrade, L. H., & Porto, A. L. M. (2007). Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry, 18( 9), 1070-1076.
    • NLM

      Ferraz HMC, Bianco GG, Teixeira CC, Andrade LH, Porto ALM. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1070-1076.[citado 2024 out. 06 ]
    • Vancouver

      Ferraz HMC, Bianco GG, Teixeira CC, Andrade LH, Porto ALM. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1070-1076.[citado 2024 out. 06 ]
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: ANTIFÚNGICOS (ATIVIDADE), CANDIDA, PRODUTOS NATURAIS

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      REIGADA, Juliana Beltrame et al. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 18, n. 9, p. 1054-1058, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.05.006. Acesso em: 06 out. 2024.
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      Reigada, J. B., Tcacenco, C. M., Andrade, L. H., Kato, M. J., Porto, A. L. M., & Lago, J. H. G. (2007). Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 18( 9), 1054-1058. doi:10.1016/j.tetasy.2007.05.006
    • NLM

      Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
    • Vancouver

      Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidades: IQ, IQSC

    Subjects: BIOTRANSFORMAÇÃO, ASPERGILLUS

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      DA COSTA, Carlos Eduardo et al. Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus. Journal of Molecular Catalysis B - Enzymatic, v. 45, n. 3-4, p. 135-139, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2007.01.004. Acesso em: 06 out. 2024.
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      Da Costa, C. E., Comasseto, J. V., Schoenlein-Crusius, I. H., Andrade, L. H., & Porto, A. L. M. (2007). Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus. Journal of Molecular Catalysis B - Enzymatic, 45( 3-4), 135-139. doi:10.1016/j.molcatb.2007.01.004
    • NLM

      Da Costa CE, Comasseto JV, Schoenlein-Crusius IH, Andrade LH, Porto ALM. Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2007 ; 45( 3-4): 135-139.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.molcatb.2007.01.004
    • Vancouver

      Da Costa CE, Comasseto JV, Schoenlein-Crusius IH, Andrade LH, Porto ALM. Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2007 ; 45( 3-4): 135-139.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.molcatb.2007.01.004
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: BOTÂNICA, QUÍMICA

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      PIOVAN, Leandro et al. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes. Tetrahedron - Asymmetry, v. 18, n. 12, p. 1398-1402, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.05.036. Acesso em: 06 out. 2024.
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      Piovan, L., Capelari, M., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes. Tetrahedron - Asymmetry, 18( 12), 1398-1402. doi:10.1016/j.tetasy.2007.05.036
    • NLM

      Piovan L, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 12): 1398-1402.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
    • Vancouver

      Piovan L, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 12): 1398-1402.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
  • Source: Polyhedron. Unidades: IQ, IQSC

    Subjects: CRISTALOGRAFIA FÍSICA, CRISTALOGRAFIA QUÍMICA

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      TEOTONIO, Ercules Epaminondas Sousa et al. Synthesis and luminescent properties of 'Eu POT.3+'- complexes with 2-acyl-1,3-indandiontes (acind) and tppo ligands: the first x-ray structure of eu-acind complex. Polyhedron, v. 25, n. 18, p. 3488-3494, 2006Tradução . . Disponível em: http://www.sciencedirect.com/science/journal/02775387. Acesso em: 06 out. 2024.
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      Teotonio, E. E. S., Brito, H. F. de, Viertler, H., Faustino, W. M., Malta, O. L., Sá, G. F. de, et al. (2006). Synthesis and luminescent properties of 'Eu POT.3+'- complexes with 2-acyl-1,3-indandiontes (acind) and tppo ligands: the first x-ray structure of eu-acind complex. Polyhedron, 25( 18), 3488-3494. Recuperado de http://www.sciencedirect.com/science/journal/02775387
    • NLM

      Teotonio EES, Brito HF de, Viertler H, Faustino WM, Malta OL, Sá GF de, Felinto MCF da C, Santos RH de A, Cremona M. Synthesis and luminescent properties of 'Eu POT.3+'- complexes with 2-acyl-1,3-indandiontes (acind) and tppo ligands: the first x-ray structure of eu-acind complex [Internet]. Polyhedron. 2006 ; 25( 18): 3488-3494.[citado 2024 out. 06 ] Available from: http://www.sciencedirect.com/science/journal/02775387
    • Vancouver

      Teotonio EES, Brito HF de, Viertler H, Faustino WM, Malta OL, Sá GF de, Felinto MCF da C, Santos RH de A, Cremona M. Synthesis and luminescent properties of 'Eu POT.3+'- complexes with 2-acyl-1,3-indandiontes (acind) and tppo ligands: the first x-ray structure of eu-acind complex [Internet]. Polyhedron. 2006 ; 25( 18): 3488-3494.[citado 2024 out. 06 ] Available from: http://www.sciencedirect.com/science/journal/02775387
  • Source: Polyhedron. Unidades: IQ, IQSC

    Subjects: OXIDAÇÃO, ESPECTROSCOPIA RAMAN

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      SANT'ANA, Antonio Carlos et al. The adsorption of 2,2 ': 6 ',2 ''-terpyridine, 4 '-(5-mercaptopentyl)2,2 ': 6 ',2 ''-terpyridinyl, and perchlorate on silver and copper surfaces monitored by SERS. Polyhedron, v. 22, n. 13, p. 1673-1682, 2003Tradução . . Acesso em: 06 out. 2024.
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      Sant'Ana, A. C., Alves, W. A., Santos, R. H. de A., Ferreira, A. M. da C., & Temperini, M. L. A. (2003). The adsorption of 2,2 ': 6 ',2 ''-terpyridine, 4 '-(5-mercaptopentyl)2,2 ': 6 ',2 ''-terpyridinyl, and perchlorate on silver and copper surfaces monitored by SERS. Polyhedron, 22( 13), 1673-1682.
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      Sant'Ana AC, Alves WA, Santos RH de A, Ferreira AM da C, Temperini MLA. The adsorption of 2,2 ': 6 ',2 ''-terpyridine, 4 '-(5-mercaptopentyl)2,2 ': 6 ',2 ''-terpyridinyl, and perchlorate on silver and copper surfaces monitored by SERS. Polyhedron. 2003 ; 22( 13): 1673-1682.[citado 2024 out. 06 ]
    • Vancouver

      Sant'Ana AC, Alves WA, Santos RH de A, Ferreira AM da C, Temperini MLA. The adsorption of 2,2 ': 6 ',2 ''-terpyridine, 4 '-(5-mercaptopentyl)2,2 ': 6 ',2 ''-terpyridinyl, and perchlorate on silver and copper surfaces monitored by SERS. Polyhedron. 2003 ; 22( 13): 1673-1682.[citado 2024 out. 06 ]

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