Filtros : "Indexado no EMBASE" "Andrade, Leandro Helgueira" Limpar

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  • Source: Tetrahedron Asymmetry. Unidade: IQ

    Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA

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      ANDRADE, Leandro Helgueira e PIOVAN, Leandro e PASQUINI, Mônica D`Arcadia. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, v. 20, n. 13, p. 1521-1525, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.05.033. Acesso em: 12 jun. 2024.
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      Andrade, L. H., Piovan, L., & Pasquini, M. D. `A. (2009). Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, 20( 13), 1521-1525. doi:10.1016/j.tetasy.2009.05.033
    • NLM

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
    • Vancouver

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: AMINAS (COMPOSTOS ORGÂNICOS), REAGENTES ORGÂNICOS

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      ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira. First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, v. 19, n. 10, p. 1175-1181, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.04.026. Acesso em: 12 jun. 2024.
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      Andrade, L. H., & Silva, A. V. (2008). First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, 19( 10), 1175-1181. doi:10.1016/j.tetasy.2008.04.026
    • NLM

      Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
    • Vancouver

      Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
  • 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: 12 jun. 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 jun. 12 ] 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 jun. 12 ] 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: 12 jun. 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 jun. 12 ] 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 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • 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: 12 jun. 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 jun. 12 ]
    • 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 jun. 12 ]
  • 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: 12 jun. 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 jun. 12 ] 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 jun. 12 ] 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: 12 jun. 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 jun. 12 ] 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 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2007.01.004
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidade: IQ

    Subjects: BIOTRANSFORMAÇÃO, ASPERGILLUS

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      COMASSETO, João Valdir et al. Biotransformations of ortho-, meta- and para-aromatic nitrocompounds by strains of Aspergillus terreus: reduction of ketones and deracemization of alcohols. Journal of Molecular Catalysis B - Enzymatic, v. 39, n. 1-4, p. 24-30, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2006.01.022. Acesso em: 12 jun. 2024.
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      Comasseto, J. V., Assis, L. F., Andrade, L. H., Schoenlein-Crusius, I. H., & Porto, A. L. M. (2006). Biotransformations of ortho-, meta- and para-aromatic nitrocompounds by strains of Aspergillus terreus: reduction of ketones and deracemization of alcohols. Journal of Molecular Catalysis B - Enzymatic, 39( 1-4), 24-30. doi:10.1016/j.molcatb.2006.01.022
    • NLM

      Comasseto JV, Assis LF, Andrade LH, Schoenlein-Crusius IH, Porto ALM. Biotransformations of ortho-, meta- and para-aromatic nitrocompounds by strains of Aspergillus terreus: reduction of ketones and deracemization of alcohols [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2006 ; 39( 1-4): 24-30.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2006.01.022
    • Vancouver

      Comasseto JV, Assis LF, Andrade LH, Schoenlein-Crusius IH, Porto ALM. Biotransformations of ortho-, meta- and para-aromatic nitrocompounds by strains of Aspergillus terreus: reduction of ketones and deracemization of alcohols [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2006 ; 39( 1-4): 24-30.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2006.01.022
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidade: IQ

    Subjects: BIOTRANSFORMAÇÃO, REAÇÕES ORGÂNICAS

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      ANDRADE, Leandro Helgueira et al. Edible catalysts for clean chemical reactions: bioreduction of aromatic ketones and biooxidation of secondary alcohols using plants. Journal of Molecular Catalysis B - Enzymatic, v. 38, n. 2, p. 84-90, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2005.11.009. Acesso em: 12 jun. 2024.
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      Andrade, L. H., Utsunomiya, R. S., Omori, Á. T., Porto, A. L. M., & Comasseto, J. V. (2006). Edible catalysts for clean chemical reactions: bioreduction of aromatic ketones and biooxidation of secondary alcohols using plants. Journal of Molecular Catalysis B - Enzymatic, 38( 2), 84-90. doi:10.1016/j.molcatb.2005.11.009
    • NLM

      Andrade LH, Utsunomiya RS, Omori ÁT, Porto ALM, Comasseto JV. Edible catalysts for clean chemical reactions: bioreduction of aromatic ketones and biooxidation of secondary alcohols using plants [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2006 ; 38( 2): 84-90.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2005.11.009
    • Vancouver

      Andrade LH, Utsunomiya RS, Omori ÁT, Porto ALM, Comasseto JV. Edible catalysts for clean chemical reactions: bioreduction of aromatic ketones and biooxidation of secondary alcohols using plants [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2006 ; 38( 2): 84-90.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2005.11.009
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, QUÍMICA ORGÂNICA

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      VIEIRA, Tiago de Oliveira et al. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 17, n. 13, p. 1990-1994, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.014. Acesso em: 12 jun. 2024.
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      Vieira, T. de O., Ferraz, H. M. C., Andrade, L. H., & Porto, A. L. M. (2006). Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 17( 13), 1990-1994. doi:10.1016/j.tetasy.2006.07.014
    • NLM

      Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
    • Vancouver

      Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
  • Source: Enzyme and Microbial Technology. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, ASPERGILLUS, BIOTRANSFORMAÇÃO

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      KEPPLER, Artur Franz et al. Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones. Enzyme and Microbial Technology, v. 36, n. 7, p. 967-975, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2005.01.024. Acesso em: 12 jun. 2024.
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      Keppler, A. F., Porto, A. L. M., Schoenlein-Crusius, I. H., Comasseto, J. V., & Andrade, L. H. (2005). Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones. Enzyme and Microbial Technology, 36( 7), 967-975. doi:10.1016/j.enzmictec.2005.01.024
    • NLM

      Keppler AF, Porto ALM, Schoenlein-Crusius IH, Comasseto JV, Andrade LH. Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones [Internet]. Enzyme and Microbial Technology. 2005 ; 36( 7): 967-975.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.enzmictec.2005.01.024
    • Vancouver

      Keppler AF, Porto ALM, Schoenlein-Crusius IH, Comasseto JV, Andrade LH. Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones [Internet]. Enzyme and Microbial Technology. 2005 ; 36( 7): 967-975.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.enzmictec.2005.01.024
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, ASPERGILLUS, REDUÇÃO

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      COMASSETO, João Valdir et al. Deracemization of aryl ethanols and reduction of acetophenones by whole fungal cells of Aspergillus terreus CCT 4083, A.terreus CCT 3320 and Rhizopus oryzae CCT 4964. Journal of Molecular Catalysis B - Enzymatic, v. 29, n. 1-6, p. 55-61, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2004.01.015. Acesso em: 12 jun. 2024.
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      Comasseto, J. V., Andrade, L. H., Omori, Á. T., Assis, L. F., & Porto, A. L. M. (2004). Deracemization of aryl ethanols and reduction of acetophenones by whole fungal cells of Aspergillus terreus CCT 4083, A.terreus CCT 3320 and Rhizopus oryzae CCT 4964. Journal of Molecular Catalysis B - Enzymatic, 29( 1-6), 55-61. doi:10.1016/j.molcatb.2004.01.015
    • NLM

      Comasseto JV, Andrade LH, Omori ÁT, Assis LF, Porto ALM. Deracemization of aryl ethanols and reduction of acetophenones by whole fungal cells of Aspergillus terreus CCT 4083, A.terreus CCT 3320 and Rhizopus oryzae CCT 4964 [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2004 ; 29( 1-6): 55-61.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2004.01.015
    • Vancouver

      Comasseto JV, Andrade LH, Omori ÁT, Assis LF, Porto ALM. Deracemization of aryl ethanols and reduction of acetophenones by whole fungal cells of Aspergillus terreus CCT 4083, A.terreus CCT 3320 and Rhizopus oryzae CCT 4964 [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2004 ; 29( 1-6): 55-61.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2004.01.015
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidade: IQ

    Subjects: SELÊNIO, ÁLCOOL, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      ANDRADE, Leandro Helgueira et al. Asymmetric synthesis of arylselenoalcohols by means of the reduction of organoseleno acetophenones by whole fungal cells. Journal of Molecular Catalysis B - Enzymatic, v. 29, n. 1-6, p. 47-54, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2004.01.014. Acesso em: 12 jun. 2024.
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      Andrade, L. H., Omori, Á. T., Porto, A. L. M., & Comasseto, J. V. (2004). Asymmetric synthesis of arylselenoalcohols by means of the reduction of organoseleno acetophenones by whole fungal cells. Journal of Molecular Catalysis B - Enzymatic, 29( 1-6), 47-54. doi:10.1016/j.molcatb.2004.01.014
    • NLM

      Andrade LH, Omori ÁT, Porto ALM, Comasseto JV. Asymmetric synthesis of arylselenoalcohols by means of the reduction of organoseleno acetophenones by whole fungal cells [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2004 ; 29( 1-6): 47-54.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2004.01.014
    • Vancouver

      Andrade LH, Omori ÁT, Porto ALM, Comasseto JV. Asymmetric synthesis of arylselenoalcohols by means of the reduction of organoseleno acetophenones by whole fungal cells [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2004 ; 29( 1-6): 47-54.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2004.01.014
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: QUÍMICA FINA, CANDIDA, LIPASE

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      RAMINELLI, Cristiano et al. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435). Tetrahedron - Asymmetry, v. 15, n. 19, p. 3117-3122, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2004.08.022. Acesso em: 12 jun. 2024.
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      Raminelli, C., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2004). Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435). Tetrahedron - Asymmetry, 15( 19), 3117-3122. doi:10.1016/j.tetasy.2004.08.022
    • NLM

      Raminelli C, Comasseto JV, Andrade LH, Porto ALM. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435) [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 19): 3117-3122.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2004.08.022
    • Vancouver

      Raminelli C, Comasseto JV, Andrade LH, Porto ALM. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435) [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 19): 3117-3122.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2004.08.022
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidade: IQ

    Subjects: BIOTRANSFORMAÇÃO, FUNGOS, QUÍMICA ORGÂNICA

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      ANDRADE, Leandro Helgueira et al. Evaluation of acetophenone monooxygenase and alcohol dehydrogenase activities in different fungal strains by biotransformation of acetophenone derivatives. Journal of Molecular Catalysis B - Enzymatic, v. 31, n. 4-6, p. 129-135, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2004.08.006. Acesso em: 12 jun. 2024.
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      Andrade, L. H., Keppler, A. F., Schoenlein-Crusius, I. H., Porto, A. L. M., & Comasseto, J. V. (2004). Evaluation of acetophenone monooxygenase and alcohol dehydrogenase activities in different fungal strains by biotransformation of acetophenone derivatives. Journal of Molecular Catalysis B - Enzymatic, 31( 4-6), 129-135. doi:10.1016/j.molcatb.2004.08.006
    • NLM

      Andrade LH, Keppler AF, Schoenlein-Crusius IH, Porto ALM, Comasseto JV. Evaluation of acetophenone monooxygenase and alcohol dehydrogenase activities in different fungal strains by biotransformation of acetophenone derivatives [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2004 ; 31( 4-6): 129-135.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2004.08.006
    • Vancouver

      Andrade LH, Keppler AF, Schoenlein-Crusius IH, Porto ALM, Comasseto JV. Evaluation of acetophenone monooxygenase and alcohol dehydrogenase activities in different fungal strains by biotransformation of acetophenone derivatives [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2004 ; 31( 4-6): 129-135.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/j.molcatb.2004.08.006
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: ASPERGILLUS, ASSIMETRIA (REDUÇÃO), QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      COMASSETO, João Valdir et al. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae. Tetrahedron - Asymmetry, v. 14, n. 6, p. 711-715, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0957-4166(03)00096-x. Acesso em: 12 jun. 2024.
    • APA

      Comasseto, J. V., Omori, Á. T., Andrade, L. H., & Porto, A. L. M. (2003). Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae. Tetrahedron - Asymmetry, 14( 6), 711-715. doi:10.1016/s0957-4166(03)00096-x
    • NLM

      Comasseto JV, Omori ÁT, Andrade LH, Porto ALM. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae [Internet]. Tetrahedron - Asymmetry. 2003 ; 14( 6): 711-715.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/s0957-4166(03)00096-x
    • Vancouver

      Comasseto JV, Omori ÁT, Andrade LH, Porto ALM. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae [Internet]. Tetrahedron - Asymmetry. 2003 ; 14( 6): 711-715.[citado 2024 jun. 12 ] Available from: https://doi.org/10.1016/s0957-4166(03)00096-x

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