Filtros : "Indexado no Chemical Abstracts" "PORTO, ANDRE LUIZ MELEIRO" Removidos: "Cuba" "Itália" "Hospital de Reabilitação de Anomalias Craniofaciais - Universidade de São Paulo - USP - Bauru - SP" Limpar

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  • Source: Journal of Molecular Catalysis B: enzymatic. Unidade: IQSC

    Assunto: CATÁLISE

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      MOUAD, Ana Maria et al. Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application. Journal of Molecular Catalysis B: enzymatic, v. 126, p. 64-68, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2016.01.002. Acesso em: 07 jul. 2024.
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      Mouad, A. M., Taupin, D., Lehr, L., Yvergnaux, F., & Porto, A. L. M. (2016). Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application. Journal of Molecular Catalysis B: enzymatic, 126, 64-68. doi:10.1016/j.molcatb.2016.01.002
    • NLM

      Mouad AM, Taupin D, Lehr L, Yvergnaux F, Porto ALM. Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application [Internet]. Journal of Molecular Catalysis B: enzymatic. 2016 ; 126 64-68.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.molcatb.2016.01.002
    • Vancouver

      Mouad AM, Taupin D, Lehr L, Yvergnaux F, Porto ALM. Aminolysis of linoleic and salicylic acid derivatives with Candida antarctica lipase B: A solvent-free process to obtain amphiphilic amides for cosmetic application [Internet]. Journal of Molecular Catalysis B: enzymatic. 2016 ; 126 64-68.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.molcatb.2016.01.002
  • Source: Tetrahedron. Unidade: IQSC

    Subjects: FUNGOS, QUÍMICA ORGÂNICA

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      JIMENEZ, David Esteban Quintero et al. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, v. 72, n. 46, p. 7317-7322, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2016.02.014. Acesso em: 07 jul. 2024.
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      Jimenez, D. E. Q., Ferreira , I. M., Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2016). Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, 72( 46), 7317-7322. doi:10.1016/j.tet.2016.02.014
    • NLM

      Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
    • Vancouver

      Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
  • Source: Biocatalysis and Agricultural Biotechnology. Unidade: IQSC

    Assunto: BIODEGRADAÇÃO

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      RODRIGUES, Gisele N et al. Biotransformation of methyl parathion by marine-derived fungi isolated from ascidian Didemnum ligulum. Biocatalysis and Agricultural Biotechnology, v. 7, p. 24-30, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.bcab.2016.05.001. Acesso em: 07 jul. 2024.
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      Rodrigues, G. N., Alvarenga, N., Vacondio, B., Vasconcellos, S. P. de, Passarini, M. R. Z., Seleghim, M. H. R., & Porto, A. L. M. (2016). Biotransformation of methyl parathion by marine-derived fungi isolated from ascidian Didemnum ligulum. Biocatalysis and Agricultural Biotechnology, 7, 24-30. doi:10.1016/j.bcab.2016.05.001
    • NLM

      Rodrigues GN, Alvarenga N, Vacondio B, Vasconcellos SP de, Passarini MRZ, Seleghim MHR, Porto ALM. Biotransformation of methyl parathion by marine-derived fungi isolated from ascidian Didemnum ligulum [Internet]. Biocatalysis and Agricultural Biotechnology. 2016 ; 7 24-30.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.bcab.2016.05.001
    • Vancouver

      Rodrigues GN, Alvarenga N, Vacondio B, Vasconcellos SP de, Passarini MRZ, Seleghim MHR, Porto ALM. Biotransformation of methyl parathion by marine-derived fungi isolated from ascidian Didemnum ligulum [Internet]. Biocatalysis and Agricultural Biotechnology. 2016 ; 7 24-30.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.bcab.2016.05.001
  • Source: Biotechnology Advances. Unidades: IQ, IQSC

    Subjects: QUÍMICA, ENZIMAS

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      BIROLLI, Willian Garcia et al. Biocatalysis and biotransformation in Brazil: an overview. Biotechnology Advances, v. 33, p. 481-510, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.biotechadv.2015.02.001. Acesso em: 07 jul. 2024.
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      Birolli, W. G., Ferreira , I. M., Alvarenga, N., Matos, I. L. de, Comasseto, J. V., & Porto, A. L. M. (2015). Biocatalysis and biotransformation in Brazil: an overview. Biotechnology Advances, 33, 481-510. doi:10.1016/j.biotechadv.2015.02.001
    • NLM

      Birolli WG, Ferreira IM, Alvarenga N, Matos IL de, Comasseto JV, Porto ALM. Biocatalysis and biotransformation in Brazil: an overview [Internet]. Biotechnology Advances. 2015 ; 33 481-510.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.biotechadv.2015.02.001
    • Vancouver

      Birolli WG, Ferreira IM, Alvarenga N, Matos IL de, Comasseto JV, Porto ALM. Biocatalysis and biotransformation in Brazil: an overview [Internet]. Biotechnology Advances. 2015 ; 33 481-510.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.biotechadv.2015.02.001
  • Source: Biocatalysis and Agricultural Biotechnology. Unidade: IQSC

    Subjects: MICROBIOLOGIA, PENICILLIUM

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      BIROLLI, Willian Garcia et al. Biotransformation of dieldrin by the marine fungus Penicillium miczynskii CBMAI 930. Biocatalysis and Agricultural Biotechnology, v. 4, p. 39-43, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.bcab.2014.06.002. Acesso em: 07 jul. 2024.
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      Birolli, W. G., Yamamoto, K. Y., Oliveira, J. R. de, Nitschke, M., Seleghim, M. H. R., & Porto, A. L. M. (2015). Biotransformation of dieldrin by the marine fungus Penicillium miczynskii CBMAI 930. Biocatalysis and Agricultural Biotechnology, 4, 39-43. doi:10.1016/j.bcab.2014.06.002
    • NLM

      Birolli WG, Yamamoto KY, Oliveira JR de, Nitschke M, Seleghim MHR, Porto ALM. Biotransformation of dieldrin by the marine fungus Penicillium miczynskii CBMAI 930 [Internet]. Biocatalysis and Agricultural Biotechnology. 2015 ; 4 39-43.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.bcab.2014.06.002
    • Vancouver

      Birolli WG, Yamamoto KY, Oliveira JR de, Nitschke M, Seleghim MHR, Porto ALM. Biotransformation of dieldrin by the marine fungus Penicillium miczynskii CBMAI 930 [Internet]. Biocatalysis and Agricultural Biotechnology. 2015 ; 4 39-43.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.bcab.2014.06.002
  • Source: Marine Biotechnology. Unidades: IQSC, FCFRP

    Subjects: FUNGOS, BIOTRANSFORMAÇÃO

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      MARTINS, Mariana Provedel et al. Biohydroxylation of (−)-Ambrox®, (−)-Sclareol, and (+)- Sclareolide by whole cells of brazilian marine-derived fungi. Marine Biotechnology, v. 17, n. 2, p. 211-218, 2015Tradução . . Disponível em: https://doi.org/10.1007/s10126-015-9610-7. Acesso em: 07 jul. 2024.
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      Martins, M. P., Ouazzani, J., Arcile, G., Jeller, A. H., Lima, J. P. F. de, Seleghim, M. H. R., et al. (2015). Biohydroxylation of (−)-Ambrox®, (−)-Sclareol, and (+)- Sclareolide by whole cells of brazilian marine-derived fungi. Marine Biotechnology, 17( 2), 211-218. doi:10.1007/s10126-015-9610-7
    • NLM

      Martins MP, Ouazzani J, Arcile G, Jeller AH, Lima JPF de, Seleghim MHR, Oliveira ALL de, Debonsi HM, Venâncio T, Yokoya NS, Fujii MT, Porto ALM. Biohydroxylation of (−)-Ambrox®, (−)-Sclareol, and (+)- Sclareolide by whole cells of brazilian marine-derived fungi [Internet]. Marine Biotechnology. 2015 ; 17( 2): 211-218.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-015-9610-7
    • Vancouver

      Martins MP, Ouazzani J, Arcile G, Jeller AH, Lima JPF de, Seleghim MHR, Oliveira ALL de, Debonsi HM, Venâncio T, Yokoya NS, Fujii MT, Porto ALM. Biohydroxylation of (−)-Ambrox®, (−)-Sclareol, and (+)- Sclareolide by whole cells of brazilian marine-derived fungi [Internet]. Marine Biotechnology. 2015 ; 17( 2): 211-218.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-015-9610-7
  • Source: Journal of Molecular Catalysis B: Enzymatic. Unidade: IQSC

    Subjects: QUÍMICA, ENZIMAS

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      FERREIRA, Irlon Maciel et al. Chemoselective biohydrogenation of α,β- and α,β,γ,δ-unsaturated ketones by the marine-derived fungus Penicillium citrinum CBMAI 1186 in a biphasic system. Journal of Molecular Catalysis B: Enzymatic, v. 115, n. 1, p. 59-65, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2015.01.017. Acesso em: 07 jul. 2024.
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      Ferreira, I. M., Meira, E. B., Rosset, I. G., & Porto, A. L. M. (2015). Chemoselective biohydrogenation of α,β- and α,β,γ,δ-unsaturated ketones by the marine-derived fungus Penicillium citrinum CBMAI 1186 in a biphasic system. Journal of Molecular Catalysis B: Enzymatic, 115( 1), 59-65. doi:10.1016/j.molcatb.2015.01.017
    • NLM

      Ferreira IM, Meira EB, Rosset IG, Porto ALM. Chemoselective biohydrogenation of α,β- and α,β,γ,δ-unsaturated ketones by the marine-derived fungus Penicillium citrinum CBMAI 1186 in a biphasic system [Internet]. Journal of Molecular Catalysis B: Enzymatic. 2015 ; 115( 1): 59-65.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.molcatb.2015.01.017
    • Vancouver

      Ferreira IM, Meira EB, Rosset IG, Porto ALM. Chemoselective biohydrogenation of α,β- and α,β,γ,δ-unsaturated ketones by the marine-derived fungus Penicillium citrinum CBMAI 1186 in a biphasic system [Internet]. Journal of Molecular Catalysis B: Enzymatic. 2015 ; 115( 1): 59-65.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.molcatb.2015.01.017
  • Source: Marine Biotechnology. Unidade: IQSC

    Assunto: FUNGOS

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      ROCHA, Lenilson C et al. Stereoselective bioreduction of azido ketones by whole cells of marine derived fungi. Marine Biotechnology, v. 17, p. 736-742, 2015Tradução . . Disponível em: https://doi.org/10.1007/s10126-015-9644-x. Acesso em: 07 jul. 2024.
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      Rocha, L. C., Seleghim, M. H. R., Comasseto, J. V., Sette, L. D., & Porto, A. L. M. (2015). Stereoselective bioreduction of azido ketones by whole cells of marine derived fungi. Marine Biotechnology, 17, 736-742. doi:10.1007/s10126-015-9644-x
    • NLM

      Rocha LC, Seleghim MHR, Comasseto JV, Sette LD, Porto ALM. Stereoselective bioreduction of azido ketones by whole cells of marine derived fungi [Internet]. Marine Biotechnology. 2015 ; 17 736-742.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-015-9644-x
    • Vancouver

      Rocha LC, Seleghim MHR, Comasseto JV, Sette LD, Porto ALM. Stereoselective bioreduction of azido ketones by whole cells of marine derived fungi [Internet]. Marine Biotechnology. 2015 ; 17 736-742.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-015-9644-x
  • Source: Current Organic Synthesis. Unidades: IQ, IQSC

    Assunto: SÍNTESE ORGÂNICA

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      ANDRADE, Leandro Helgueira et al. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil. Current Organic Synthesis, v. 12, p. 696-713, 2015Tradução . . Disponível em: https://doi.org/10.2174/157017941206150828103404. Acesso em: 07 jul. 2024.
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      Andrade, L. H., Sousa, B. A., Ferreira , I. M., & Porto, A. L. M. (2015). Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil. Current Organic Synthesis, 12, 696-713. doi:10.2174/157017941206150828103404
    • NLM

      Andrade LH, Sousa BA, Ferreira IM, Porto ALM. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil [Internet]. Current Organic Synthesis. 2015 ; 12 696-713.[citado 2024 jul. 07 ] Available from: https://doi.org/10.2174/157017941206150828103404
    • Vancouver

      Andrade LH, Sousa BA, Ferreira IM, Porto ALM. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil [Internet]. Current Organic Synthesis. 2015 ; 12 696-713.[citado 2024 jul. 07 ] Available from: https://doi.org/10.2174/157017941206150828103404
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Subjects: LIPASE, QUÍMICA ORGÂNICA

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      COSTA, José A. S. et al. A new functionalized MCM-41 mesoporous material for use in environmental applications. Journal of the Brazilian Chemical Society, v. 25, n. 2, p. 197-207, 2014Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20130284. Acesso em: 07 jul. 2024.
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      Costa, J. A. S., Garcia, A. C. F. S., Santos, D. O., Sarmento, V. H. V., Porto, A. L. M., Mesquita, M. E. de, & Romão, L. P. C. (2014). A new functionalized MCM-41 mesoporous material for use in environmental applications. Journal of the Brazilian Chemical Society, 25( 2), 197-207. doi:10.5935/0103-5053.20130284
    • NLM

      Costa JAS, Garcia ACFS, Santos DO, Sarmento VHV, Porto ALM, Mesquita ME de, Romão LPC. A new functionalized MCM-41 mesoporous material for use in environmental applications [Internet]. Journal of the Brazilian Chemical Society. 2014 ; 25( 2): 197-207.[citado 2024 jul. 07 ] Available from: https://doi.org/10.5935/0103-5053.20130284
    • Vancouver

      Costa JAS, Garcia ACFS, Santos DO, Sarmento VHV, Porto ALM, Mesquita ME de, Romão LPC. A new functionalized MCM-41 mesoporous material for use in environmental applications [Internet]. Journal of the Brazilian Chemical Society. 2014 ; 25( 2): 197-207.[citado 2024 jul. 07 ] Available from: https://doi.org/10.5935/0103-5053.20130284
  • Source: Journal of Microbial & Biochemical Technology. Unidade: IQSC

    Subjects: ENZIMAS HIDROLÍTICAS, BIODEGRADAÇÃO

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      BIROLLI, Willian Garcia et al. Growth assessment of marine-derived fungi in the presence of esfenvalerate and its main metabolites. Journal of Microbial & Biochemical Technology, v. 6, n. 5, p. 260-267, 2014Tradução . . Disponível em: https://doi.org/10.4172/1948-5948.1000154. Acesso em: 07 jul. 2024.
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      Birolli, W. G., Alvarenga, N., Vacondio, B., Seleghim, M. H. R., & Porto, A. L. M. (2014). Growth assessment of marine-derived fungi in the presence of esfenvalerate and its main metabolites. Journal of Microbial & Biochemical Technology, 6( 5), 260-267. doi:10.4172/1948-5948.1000154
    • NLM

      Birolli WG, Alvarenga N, Vacondio B, Seleghim MHR, Porto ALM. Growth assessment of marine-derived fungi in the presence of esfenvalerate and its main metabolites [Internet]. Journal of Microbial & Biochemical Technology. 2014 ; 6( 5): 260-267.[citado 2024 jul. 07 ] Available from: https://doi.org/10.4172/1948-5948.1000154
    • Vancouver

      Birolli WG, Alvarenga N, Vacondio B, Seleghim MHR, Porto ALM. Growth assessment of marine-derived fungi in the presence of esfenvalerate and its main metabolites [Internet]. Journal of Microbial & Biochemical Technology. 2014 ; 6( 5): 260-267.[citado 2024 jul. 07 ] Available from: https://doi.org/10.4172/1948-5948.1000154
  • Source: Tetrahedron Letters. Unidades: FCFRP, IQSC

    Subjects: ENZIMAS, QUÍMICA ORGÂNICA

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      FERREIRA , Irlon Maciel et al. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres. Tetrahedron Letters, v. 55, n. 7, p. 5062-5065, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.07.032. Acesso em: 07 jul. 2024.
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      Ferreira , I. M., Nishimura, R. H. V., Souza, A. B. dos A., Clososki, G. C., Yoshioka, S. A., & Porto, A. L. M. (2014). Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres. Tetrahedron Letters, 55( 7), 5062-5065. doi:10.1016/j.tetlet.2014.07.032
    • NLM

      Ferreira IM, Nishimura RHV, Souza AB dos A, Clososki GC, Yoshioka SA, Porto ALM. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres [Internet]. Tetrahedron Letters. 2014 ; 55( 7): 5062-5065.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2014.07.032
    • Vancouver

      Ferreira IM, Nishimura RHV, Souza AB dos A, Clososki GC, Yoshioka SA, Porto ALM. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres [Internet]. Tetrahedron Letters. 2014 ; 55( 7): 5062-5065.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2014.07.032
  • Source: Current Microwave Chemistry. Unidade: IQSC

    Assunto: QUÍMICA VERDE

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      ARAUJO, Yara Jaqueline Kerber e PORTO, Andre Luiz Meleiro. Aza-Michael addittion of primary amines by lipases and microwave irradiation: a green protocol for the synthesis of propanenitrile derivatives. Current Microwave Chemistry, v. 1, n. 2, p. 1-7, 2014Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/fcf731d7-5e3f-41c7-979c-a9a5c630747c/P15157.pdf. Acesso em: 07 jul. 2024.
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      Araujo, Y. J. K., & Porto, A. L. M. (2014). Aza-Michael addittion of primary amines by lipases and microwave irradiation: a green protocol for the synthesis of propanenitrile derivatives. Current Microwave Chemistry, 1( 2), 1-7. Recuperado de https://repositorio.usp.br/directbitstream/fcf731d7-5e3f-41c7-979c-a9a5c630747c/P15157.pdf
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      Araujo YJK, Porto ALM. Aza-Michael addittion of primary amines by lipases and microwave irradiation: a green protocol for the synthesis of propanenitrile derivatives [Internet]. Current Microwave Chemistry. 2014 ; 1( 2): 1-7.[citado 2024 jul. 07 ] Available from: https://repositorio.usp.br/directbitstream/fcf731d7-5e3f-41c7-979c-a9a5c630747c/P15157.pdf
    • Vancouver

      Araujo YJK, Porto ALM. Aza-Michael addittion of primary amines by lipases and microwave irradiation: a green protocol for the synthesis of propanenitrile derivatives [Internet]. Current Microwave Chemistry. 2014 ; 1( 2): 1-7.[citado 2024 jul. 07 ] Available from: https://repositorio.usp.br/directbitstream/fcf731d7-5e3f-41c7-979c-a9a5c630747c/P15157.pdf
  • Source: Biocatalysis and Agricultural Biotechnology. Unidade: IQSC

    Assunto: QUÍMICA ORGÂNICA

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      FERREIRA , Irlon Maciel et al. Chemoselective reduction of chalcones by whole hyphae of marine fungus penicillium citrinum CBMAI 1186, free and immobilized on biopolymers. Biocatalysis and Agricultural Biotechnology, v. 3, n. 4, p. 358-364, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.bcab.2014.04.001. Acesso em: 07 jul. 2024.
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      Ferreira , I. M., Rocha, L. C. da, Yoshioka, S. A., Nitschke, M., Jeller, A. H., Pizzuti, L., et al. (2014). Chemoselective reduction of chalcones by whole hyphae of marine fungus penicillium citrinum CBMAI 1186, free and immobilized on biopolymers. Biocatalysis and Agricultural Biotechnology, 3( 4), 358-364. doi:10.1016/j.bcab.2014.04.001
    • NLM

      Ferreira IM, Rocha LC da, Yoshioka SA, Nitschke M, Jeller AH, Pizzuti L, Seleghim MHR, Porto ALM. Chemoselective reduction of chalcones by whole hyphae of marine fungus penicillium citrinum CBMAI 1186, free and immobilized on biopolymers [Internet]. Biocatalysis and Agricultural Biotechnology. 2014 ; 3( 4): 358-364.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.bcab.2014.04.001
    • Vancouver

      Ferreira IM, Rocha LC da, Yoshioka SA, Nitschke M, Jeller AH, Pizzuti L, Seleghim MHR, Porto ALM. Chemoselective reduction of chalcones by whole hyphae of marine fungus penicillium citrinum CBMAI 1186, free and immobilized on biopolymers [Internet]. Biocatalysis and Agricultural Biotechnology. 2014 ; 3( 4): 358-364.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.bcab.2014.04.001
  • Source: Chemosphere. Unidade: IQSC

    Assunto: ENZIMAS HIDROLÍTICAS

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      ALVARENGA, Natália et al. Biodegradation of methyl parathion by whole cells of marine-derived fungi Aspergillus sydowii and Penicillium decaturense. Chemosphere, v. 117, p. 47-52, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.chemosphere.2014.05.069. Acesso em: 07 jul. 2024.
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      Alvarenga, N., Birolli, W. G., Seleghim, M. H. R., & Porto, A. L. M. (2014). Biodegradation of methyl parathion by whole cells of marine-derived fungi Aspergillus sydowii and Penicillium decaturense. Chemosphere, 117, 47-52. doi:10.1016/j.chemosphere.2014.05.069
    • NLM

      Alvarenga N, Birolli WG, Seleghim MHR, Porto ALM. Biodegradation of methyl parathion by whole cells of marine-derived fungi Aspergillus sydowii and Penicillium decaturense [Internet]. Chemosphere. 2014 ; 117 47-52.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.chemosphere.2014.05.069
    • Vancouver

      Alvarenga N, Birolli WG, Seleghim MHR, Porto ALM. Biodegradation of methyl parathion by whole cells of marine-derived fungi Aspergillus sydowii and Penicillium decaturense [Internet]. Chemosphere. 2014 ; 117 47-52.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1016/j.chemosphere.2014.05.069
  • Source: Marine Biotechnology. Unidade: IQSC

    Subjects: FUNGOS, BIOTRANSFORMAÇÃO

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      OLIVEIRA, Julieta Rangel de e SELEGHIM, Mirna Helena Regali e PORTO, Andre Luiz Meleiro. Biotransformation of methylphenylacetonitriles by brazilian marine fungal strain aspergillus sydowii CBMAI 934: eco-friendly reactions. Marine Biotechnology, v. 16, p. 156-160, 2014Tradução . . Disponível em: https://doi.org/10.1007/s10126-013-9534-z. Acesso em: 07 jul. 2024.
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      Oliveira, J. R. de, Seleghim, M. H. R., & Porto, A. L. M. (2014). Biotransformation of methylphenylacetonitriles by brazilian marine fungal strain aspergillus sydowii CBMAI 934: eco-friendly reactions. Marine Biotechnology, 16, 156-160. doi:10.1007/s10126-013-9534-z
    • NLM

      Oliveira JR de, Seleghim MHR, Porto ALM. Biotransformation of methylphenylacetonitriles by brazilian marine fungal strain aspergillus sydowii CBMAI 934: eco-friendly reactions [Internet]. Marine Biotechnology. 2014 ; 16 156-160.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-013-9534-z
    • Vancouver

      Oliveira JR de, Seleghim MHR, Porto ALM. Biotransformation of methylphenylacetonitriles by brazilian marine fungal strain aspergillus sydowii CBMAI 934: eco-friendly reactions [Internet]. Marine Biotechnology. 2014 ; 16 156-160.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-013-9534-z
  • Source: Marine Biotechnology. Unidade: IQSC

    Subjects: FUNGOS, BIOTRANSFORMAÇÃO

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      OLIVEIRA, Julieta Rangel de et al. Biotransformation of phenylacetonitrile to 2-hydroxyphenylacetic acid by marina fungi. Marine Biotechnology, v. 15, n. 1, p. 97-103, 2013Tradução . . Disponível em: https://doi.org/10.1007/s10126-012-9464-1. Acesso em: 07 jul. 2024.
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      Oliveira, J. R. de, Mizuno, C. M., Seleghim, M. H. R., Javaroti, D. C. D., Rezende, M. O. de O., Landgraf, M. D., et al. (2013). Biotransformation of phenylacetonitrile to 2-hydroxyphenylacetic acid by marina fungi. Marine Biotechnology, 15( 1), 97-103. doi:10.1007/s10126-012-9464-1
    • NLM

      Oliveira JR de, Mizuno CM, Seleghim MHR, Javaroti DCD, Rezende MO de O, Landgraf MD, Sette LD, Porto ALM. Biotransformation of phenylacetonitrile to 2-hydroxyphenylacetic acid by marina fungi [Internet]. Marine Biotechnology. 2013 ; 15( 1): 97-103.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-012-9464-1
    • Vancouver

      Oliveira JR de, Mizuno CM, Seleghim MHR, Javaroti DCD, Rezende MO de O, Landgraf MD, Sette LD, Porto ALM. Biotransformation of phenylacetonitrile to 2-hydroxyphenylacetic acid by marina fungi [Internet]. Marine Biotechnology. 2013 ; 15( 1): 97-103.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1007/s10126-012-9464-1
  • Source: Current Catalysis. Unidade: IQSC

    Assunto: BIODIESEL

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      ROSSET, Isac George e ASSAF, Elisabete Moreira e PORTO, Andre Luiz Meleiro. Biocatalytic production of ethyl esters (biodiesel) by enzymatic trans-esterification from synthetic triolein. Current Catalysis, v. 2, n. 1, p. 53-61, 2013Tradução . . Disponível em: https://doi.org/10.2174/2211544711302010009. Acesso em: 07 jul. 2024.
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      Rosset, I. G., Assaf, E. M., & Porto, A. L. M. (2013). Biocatalytic production of ethyl esters (biodiesel) by enzymatic trans-esterification from synthetic triolein. Current Catalysis, 2( 1), 53-61. doi:10.2174/2211544711302010009
    • NLM

      Rosset IG, Assaf EM, Porto ALM. Biocatalytic production of ethyl esters (biodiesel) by enzymatic trans-esterification from synthetic triolein [Internet]. Current Catalysis. 2013 ; 2( 1): 53-61.[citado 2024 jul. 07 ] Available from: https://doi.org/10.2174/2211544711302010009
    • Vancouver

      Rosset IG, Assaf EM, Porto ALM. Biocatalytic production of ethyl esters (biodiesel) by enzymatic trans-esterification from synthetic triolein [Internet]. Current Catalysis. 2013 ; 2( 1): 53-61.[citado 2024 jul. 07 ] Available from: https://doi.org/10.2174/2211544711302010009
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Subjects: LIPASE, QUÍMICA ORGÂNICA

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      ROCHA, Lenilson Coutinho da et al. Chemoenzymatic resolution of β-azidophenylethanols by candida antarctica and their application for the synthesis of chiral benzotriazoles. Journal of the Brazilian Chemical Society, v. 24, n. 9, p. 1427-1432 + S1-S37, 2013Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20130181. Acesso em: 07 jul. 2024.
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      Rocha, L. C. da, Rosset, I. G., Melgar, G. Z., Raminelli, C., Porto, A. L. M., & Jeller, A. H. (2013). Chemoenzymatic resolution of β-azidophenylethanols by candida antarctica and their application for the synthesis of chiral benzotriazoles. Journal of the Brazilian Chemical Society, 24( 9), 1427-1432 + S1-S37. doi:10.5935/0103-5053.20130181
    • NLM

      Rocha LC da, Rosset IG, Melgar GZ, Raminelli C, Porto ALM, Jeller AH. Chemoenzymatic resolution of β-azidophenylethanols by candida antarctica and their application for the synthesis of chiral benzotriazoles [Internet]. Journal of the Brazilian Chemical Society. 2013 ; 24( 9): 1427-1432 + S1-S37.[citado 2024 jul. 07 ] Available from: https://doi.org/10.5935/0103-5053.20130181
    • Vancouver

      Rocha LC da, Rosset IG, Melgar GZ, Raminelli C, Porto ALM, Jeller AH. Chemoenzymatic resolution of β-azidophenylethanols by candida antarctica and their application for the synthesis of chiral benzotriazoles [Internet]. Journal of the Brazilian Chemical Society. 2013 ; 24( 9): 1427-1432 + S1-S37.[citado 2024 jul. 07 ] Available from: https://doi.org/10.5935/0103-5053.20130181
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Subjects: FUNGOS, FÍSICO-QUÍMICA

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      RIBEIRO, Sandra S. e OLIVEIRA, Julieta Rangel de e PORTO, Andre Luiz Meleiro. Lipase-catalyzed kinetic resolution of (±)-mandelonitrile under conventional condition and microwave irradiation. Journal of the Brazilian Chemical Society, v. 23, n. 7, p. 1395-1399 + S1-S6, 2012Tradução . . Disponível em: https://doi.org/10.1590/S0103-50532012000700025. Acesso em: 07 jul. 2024.
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      Ribeiro, S. S., Oliveira, J. R. de, & Porto, A. L. M. (2012). Lipase-catalyzed kinetic resolution of (±)-mandelonitrile under conventional condition and microwave irradiation. Journal of the Brazilian Chemical Society, 23( 7), 1395-1399 + S1-S6. doi:10.1590/S0103-50532012000700025
    • NLM

      Ribeiro SS, Oliveira JR de, Porto ALM. Lipase-catalyzed kinetic resolution of (±)-mandelonitrile under conventional condition and microwave irradiation [Internet]. Journal of the Brazilian Chemical Society. 2012 ; 23( 7): 1395-1399 + S1-S6.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1590/S0103-50532012000700025
    • Vancouver

      Ribeiro SS, Oliveira JR de, Porto ALM. Lipase-catalyzed kinetic resolution of (±)-mandelonitrile under conventional condition and microwave irradiation [Internet]. Journal of the Brazilian Chemical Society. 2012 ; 23( 7): 1395-1399 + S1-S6.[citado 2024 jul. 07 ] Available from: https://doi.org/10.1590/S0103-50532012000700025

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