Filtros : "Indexado no Chemical Abstracts" "Porto, Andre Luiz Meleiro" Removido: "Acta Scientiarum" Limpar

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  • Source: Quimica Nova na Escola. Unidade: IQSC

    Subjects: ENSINO SUPERIOR, QUÍMICA ORGÂNICA, DIVULGAÇÃO CIENTÍFICA

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      DAMADA, Pedro Henrique e PORTO, Andre Luiz Meleiro. Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota. Quimica Nova na Escola, n. 1, p. 20-29, 2023Tradução . . Disponível em: https://doi.org/10.21577/0104-8899.20160289. Acesso em: 24 ago. 2024.
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      Damada, P. H., & Porto, A. L. M. (2023). Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota. Quimica Nova na Escola, ( 1), 20-29. doi:10.21577/0104-8899.20160289
    • NLM

      Damada PH, Porto ALM. Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota [Internet]. Quimica Nova na Escola. 2023 ;( 1): 20-29.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0104-8899.20160289
    • Vancouver

      Damada PH, Porto ALM. Aplicação de ferramentas pedagógicas na disciplina de Química Orgânica I de forma remota [Internet]. Quimica Nova na Escola. 2023 ;( 1): 20-29.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0104-8899.20160289
  • Source: Marine Pollution Bulletin. Unidade: IQSC

    Subjects: BIOTRANSFORMAÇÃO, INSETICIDAS, BIODEGRADAÇÃO, FUNGOS

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      SOARES, Paulo Roberto Serrão et al. Biodegradation pathway of the organophosphate pesticides chlorpyrifos, methyl parathion and profenofos by the marine-derived fungus Aspergillus sydowii CBMAI 935 and its potential for methylation reactions of phenolic compounds. Marine Pollution Bulletin, v. 166, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.marpolbul.2021.112185. Acesso em: 24 ago. 2024.
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      Soares, P. R. S., Birolli, W. G., Ferreira, I. M., & Porto, A. L. M. (2021). Biodegradation pathway of the organophosphate pesticides chlorpyrifos, methyl parathion and profenofos by the marine-derived fungus Aspergillus sydowii CBMAI 935 and its potential for methylation reactions of phenolic compounds. Marine Pollution Bulletin, 166. doi:10.1016/j.marpolbul.2021.112185
    • NLM

      Soares PRS, Birolli WG, Ferreira IM, Porto ALM. Biodegradation pathway of the organophosphate pesticides chlorpyrifos, methyl parathion and profenofos by the marine-derived fungus Aspergillus sydowii CBMAI 935 and its potential for methylation reactions of phenolic compounds [Internet]. Marine Pollution Bulletin. 2021 ; 166[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.marpolbul.2021.112185
    • Vancouver

      Soares PRS, Birolli WG, Ferreira IM, Porto ALM. Biodegradation pathway of the organophosphate pesticides chlorpyrifos, methyl parathion and profenofos by the marine-derived fungus Aspergillus sydowii CBMAI 935 and its potential for methylation reactions of phenolic compounds [Internet]. Marine Pollution Bulletin. 2021 ; 166[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.marpolbul.2021.112185
  • Source: Current Bioactive Compounds. Unidades: IQSC, INTER IFSC/IQSC/ICMC

    Subjects: NEOPLASIAS, ANTIOXIDANTES, BACTERICIDAS

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      LIMA, Rafaely Nascimento et al. Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines. Current Bioactive Compounds, v. 16, n. 6, p. 900-910, 2020Tradução . . Disponível em: https://doi.org/10.2174/1573407215666190318144105. Acesso em: 24 ago. 2024.
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      Lima, R. N., Gonçalves, J. R., Silva, V. R., Santos, L. de S., Bezerra, D. P., Soares, M. B. P., et al. (2020). Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines. Current Bioactive Compounds, 16( 6), 900-910. doi:10.2174/1573407215666190318144105
    • NLM

      Lima RN, Gonçalves JR, Silva VR, Santos L de S, Bezerra DP, Soares MBP, Leitão A, Porto ALM. Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines [Internet]. Current Bioactive Compounds. 2020 ; 16( 6): 900-910.[citado 2024 ago. 24 ] Available from: https://doi.org/10.2174/1573407215666190318144105
    • Vancouver

      Lima RN, Gonçalves JR, Silva VR, Santos L de S, Bezerra DP, Soares MBP, Leitão A, Porto ALM. Antioxidant, Antitumor and Bactericidal Activities of Ethyl Gallate Quinoxalines [Internet]. Current Bioactive Compounds. 2020 ; 16( 6): 900-910.[citado 2024 ago. 24 ] Available from: https://doi.org/10.2174/1573407215666190318144105
  • Source: ACS Catalysis. Unidade: IQSC

    Subjects: CATÁLISE, ALCALOIDES

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      SILVA, Natália Alvarenga da et al. Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation. ACS Catalysis, v. 10, n. 2, p. 1607-1620, 2020Tradução . . Disponível em: https://doi.org/10.1021/acscatal.9b04611. Acesso em: 24 ago. 2024.
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      Silva, N. A. da, Payer, S. E., Petermeier, P., Kohlfuerst, C., Porto, A. L. M., Schrittwieser, J. H., & Kroutil, W. (2020). Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation. ACS Catalysis, 10( 2), 1607-1620. doi:10.1021/acscatal.9b04611
    • NLM

      Silva NA da, Payer SE, Petermeier P, Kohlfuerst C, Porto ALM, Schrittwieser JH, Kroutil W. Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation [Internet]. ACS Catalysis. 2020 ; 10( 2): 1607-1620.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1021/acscatal.9b04611
    • Vancouver

      Silva NA da, Payer SE, Petermeier P, Kohlfuerst C, Porto ALM, Schrittwieser JH, Kroutil W. Asymmetric Synthesis of Dihydropinidine Enabled by Concurrent Multienzyme Catalysis and a Biocatalytic Alternative to Krapcho Dealkoxycarbonylation [Internet]. ACS Catalysis. 2020 ; 10( 2): 1607-1620.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1021/acscatal.9b04611
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Assunto: INSETICIDAS

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      ANJOS, Charlene Souza dos e BIROLLI, Willian G. e PORTO, Andre Luiz Meleiro. Biodegradation of the Pyrethroid Pesticide Esfenvalerate by a Bacterial Consortium Isolated from Brazilian Savannah. Journal of the Brazilian Chemical Society, v. 31, n. 8, p. 1654-1660, 2020Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20200051. Acesso em: 24 ago. 2024.
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      Anjos, C. S. dos, Birolli, W. G., & Porto, A. L. M. (2020). Biodegradation of the Pyrethroid Pesticide Esfenvalerate by a Bacterial Consortium Isolated from Brazilian Savannah. Journal of the Brazilian Chemical Society, 31( 8), 1654-1660. doi:10.21577/0103-5053.20200051
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      Anjos CS dos, Birolli WG, Porto ALM. Biodegradation of the Pyrethroid Pesticide Esfenvalerate by a Bacterial Consortium Isolated from Brazilian Savannah [Internet]. Journal of the Brazilian Chemical Society. 2020 ;31( 8): 1654-1660.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0103-5053.20200051
    • Vancouver

      Anjos CS dos, Birolli WG, Porto ALM. Biodegradation of the Pyrethroid Pesticide Esfenvalerate by a Bacterial Consortium Isolated from Brazilian Savannah [Internet]. Journal of the Brazilian Chemical Society. 2020 ;31( 8): 1654-1660.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0103-5053.20200051
  • Source: Marine Biotechnology. Unidades: IQSC, IFSC

    Subjects: MEIO AMBIENTE, BIOTRANSFORMAÇÃO, FUNGOS, ESTEROIDES

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      QUEIROZ, Thayane Melo de e ELLENA, Javier e PORTO, Andre Luiz Meleiro. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996. Marine Biotechnology, v. 22, n. 5, p. 673-682, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10126-020-09989-w. Acesso em: 24 ago. 2024.
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      Queiroz, T. M. de, Ellena, J., & Porto, A. L. M. (2020). Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996. Marine Biotechnology, 22( 5), 673-682. doi:10.1007/s10126-020-09989-w
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      Queiroz TM de, Ellena J, Porto ALM. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 [Internet]. Marine Biotechnology. 2020 ; 22( 5): 673-682.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-020-09989-w
    • Vancouver

      Queiroz TM de, Ellena J, Porto ALM. Biotransformation of Ethinylestradiol by Whole Cells of Brazilian Marine-Derived Fungus Penicillium oxalicum CBMAI 1996 [Internet]. Marine Biotechnology. 2020 ; 22( 5): 673-682.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-020-09989-w
  • Source: Marine Biotechnology. Unidade: IQSC

    Assunto: CATÁLISE

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      FERREIRA, Irlon Maciel et al. Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan. Marine Biotechnology, v. 22, p. 348-356, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10126-020-09954-7. Acesso em: 24 ago. 2024.
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      Ferreira, I. M., Fiamingo, A., Campana Filho, S. P., & Porto, A. L. M. (2020). Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan. Marine Biotechnology, 22, 348-356. doi:10.1007%2Fs10126-020-09954-7
    • NLM

      Ferreira IM, Fiamingo A, Campana Filho SP, Porto ALM. Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan [Internet]. Marine Biotechnology. 2020 ; 22 348-356.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-020-09954-7
    • Vancouver

      Ferreira IM, Fiamingo A, Campana Filho SP, Porto ALM. Biotransformation of (E)-2-Methyl-3-Phenylacrylaldehyde Using Mycelia of Penicillium citrinum CBMAI 1186, Both Free and Immobilized on Chitosan [Internet]. Marine Biotechnology. 2020 ; 22 348-356.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-020-09954-7
  • Source: Bioresource Technology. Unidade: IQSC

    Subjects: CATÁLISE, LIPASE

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      BIROLLI, Willian Garcia e PORTO, Andre Luiz Meleiro e FONSECA, Luís Pina. Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase. Bioresource Technology, v. 297, p. 122441, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.biortech.2019.122441. Acesso em: 24 ago. 2024.
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      Birolli, W. G., Porto, A. L. M., & Fonseca, L. P. (2020). Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase. Bioresource Technology, 297, 122441. doi:10.1016/j.biortech.2019.122441
    • NLM

      Birolli WG, Porto ALM, Fonseca LP. Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase [Internet]. Bioresource Technology. 2020 ; 297 122441.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.biortech.2019.122441
    • Vancouver

      Birolli WG, Porto ALM, Fonseca LP. Miniemulsion in biocatalysis, a new approach employing a solid reagent and an easy protocol for product isolation applied to the aldol reaction by Rhizopus niveus lipase [Internet]. Bioresource Technology. 2020 ; 297 122441.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.biortech.2019.122441
  • Source: Marine Biotechnology. Unidade: IQSC

    Assunto: CATÁLISE

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      BIROLLI, Willian Garcia et al. Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives. Marine Biotechnology, v. 22, p. 317–330, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10126-020-09953-8. Acesso em: 24 ago. 2024.
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      Birolli, W. G., Zanin, L. L., Jimenez, D. E. Q., & Porto, A. L. M. (2020). Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives. Marine Biotechnology, 22, 317–330. doi:10.1007%2Fs10126-020-09953-8
    • NLM

      Birolli WG, Zanin LL, Jimenez DEQ, Porto ALM. Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives [Internet]. Marine Biotechnology. 2020 ; 22 317–330.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-020-09953-8
    • Vancouver

      Birolli WG, Zanin LL, Jimenez DEQ, Porto ALM. Synthesis of Knoevenagel Adducts Under Microwave Irradiation and Biocatalytic Ene-Reduction by the Marine-Derived Fungus Cladosporium sp. CBMAI 1237 for the Production of 2-Cyano-3-Phenylpropanamide Derivatives [Internet]. Marine Biotechnology. 2020 ; 22 317–330.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-020-09953-8
  • Source: Marine Biotechnology. Unidade: IQSC

    Subjects: BIOTRANSFORMAÇÃO, SÍNTESE ORGÂNICA

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      MATOS, Iara Lisboa de e NITSCHKE, Marcia e PORTO, Andre Luiz Meleiro. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii. Marine Biotechnology, v. 21, p. 430-439 jun, 2019Tradução . . Disponível em: https://doi.org/10.1007/s10126-019-09893-y. Acesso em: 24 ago. 2024.
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      Matos, I. L. de, Nitschke, M., & Porto, A. L. M. (2019). Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii. Marine Biotechnology, 21, 430-439 jun. doi:10.1007/s10126-019-09893-y
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      Matos IL de, Nitschke M, Porto ALM. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii [Internet]. Marine Biotechnology. 2019 ; 21 430-439 jun.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-019-09893-y
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      Matos IL de, Nitschke M, Porto ALM. Hydrogenation of halogenated 2′- hydroxychalcones by Mycelia of Marine-derived Fungus Penicillium raistrickii [Internet]. Marine Biotechnology. 2019 ; 21 430-439 jun.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-019-09893-y
  • Source: Pesticide Biochemistry and Physiology. Unidades: BIOENGENHARIA, IQSC

    Subjects: PESTICIDAS, INSETICIDAS

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      BIROLLI, Willian Garcia et al. The pyrethroid (±)-lambda-cyhalothrin enantioselective biodegradation by a bacterial consortium. Pesticide Biochemistry and Physiology, v. 156, p. 129-137, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.pestbp.2019.02.014. Acesso em: 24 ago. 2024.
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      Birolli, W. G., Arai, M. S., Nitschke, M., & Porto, A. L. M. (2019). The pyrethroid (±)-lambda-cyhalothrin enantioselective biodegradation by a bacterial consortium. Pesticide Biochemistry and Physiology, 156, 129-137. doi:10.1016/j.pestbp.2019.02.014
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      Birolli WG, Arai MS, Nitschke M, Porto ALM. The pyrethroid (±)-lambda-cyhalothrin enantioselective biodegradation by a bacterial consortium [Internet]. Pesticide Biochemistry and Physiology. 2019 ; 156 129-137.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.pestbp.2019.02.014
    • Vancouver

      Birolli WG, Arai MS, Nitschke M, Porto ALM. The pyrethroid (±)-lambda-cyhalothrin enantioselective biodegradation by a bacterial consortium [Internet]. Pesticide Biochemistry and Physiology. 2019 ; 156 129-137.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.pestbp.2019.02.014
  • Source: Journal of the Brazilian Chemical Society. Unidades: IQSC, FCFRP

    Assunto: TERPENOS

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      JESUS, Hugo César Ramos de et al. Multiple monohydroxylation products from rac-Camphor by marine fungus Botryosphaeria sp. Isolated form marine alga Bostrychia radicans. Journal of the Brazilian Chemical Society, v. 28, n. 3, p. 498-504, 2017Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20160262. Acesso em: 24 ago. 2024.
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      Jesus, H. C. R. de, Jeller, A. H., Debonsi, H. M., Alves, P. B., & Porto, A. L. M. (2017). Multiple monohydroxylation products from rac-Camphor by marine fungus Botryosphaeria sp. Isolated form marine alga Bostrychia radicans. Journal of the Brazilian Chemical Society, 28( 3), 498-504. doi:10.21577/0103-5053.20160262
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      Jesus HCR de, Jeller AH, Debonsi HM, Alves PB, Porto ALM. Multiple monohydroxylation products from rac-Camphor by marine fungus Botryosphaeria sp. Isolated form marine alga Bostrychia radicans [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 3): 498-504.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0103-5053.20160262
    • Vancouver

      Jesus HCR de, Jeller AH, Debonsi HM, Alves PB, Porto ALM. Multiple monohydroxylation products from rac-Camphor by marine fungus Botryosphaeria sp. Isolated form marine alga Bostrychia radicans [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 3): 498-504.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0103-5053.20160262
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Assunto: QUÍMICA ORGÂNICA

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      BIROLLI, Willian Garcia et al. First Asymmetric Reduction of Isatin by Marine-Derived Fungi. Journal of the Brazilian Chemical Society, v. 28, n. 6, p. 1023-1029, 2017Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20160256. Acesso em: 24 ago. 2024.
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      Birolli, W. G., Ferreira, I. M., Jimenez, D. E. Q., Silva, B. N. M., Silva, B. V., Pinto, A. C., & Porto, A. L. M. (2017). First Asymmetric Reduction of Isatin by Marine-Derived Fungi. Journal of the Brazilian Chemical Society, 28( 6), 1023-1029. doi:10.21577/0103-5053.20160256
    • NLM

      Birolli WG, Ferreira IM, Jimenez DEQ, Silva BNM, Silva BV, Pinto AC, Porto ALM. First Asymmetric Reduction of Isatin by Marine-Derived Fungi [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 6): 1023-1029.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0103-5053.20160256
    • Vancouver

      Birolli WG, Ferreira IM, Jimenez DEQ, Silva BNM, Silva BV, Pinto AC, Porto ALM. First Asymmetric Reduction of Isatin by Marine-Derived Fungi [Internet]. Journal of the Brazilian Chemical Society. 2017 ; 28( 6): 1023-1029.[citado 2024 ago. 24 ] Available from: https://doi.org/10.21577/0103-5053.20160256
  • Source: Catalysis Letters. Unidade: IQSC

    Subjects: PROTEÍNAS, ENZIMAS PROTEOLÍTICAS

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      BIROLLI, Willian Garcia e FONSECA, Luis P e PORTO, Andre Luiz Meleiro. Aldol reactions by lipase from Rhizopus niveus, an example of unspecific protein catalysis. Catalysis Letters, v. 147, n. 2, p. 1977-1987, 2017Tradução . . Disponível em: https://doi.org/10.1007/s10562-017-2121-6. Acesso em: 24 ago. 2024.
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      Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2017). Aldol reactions by lipase from Rhizopus niveus, an example of unspecific protein catalysis. Catalysis Letters, 147( 2), 1977-1987. doi:10.1007/s10562-017-2121-6
    • NLM

      Birolli WG, Fonseca LP, Porto ALM. Aldol reactions by lipase from Rhizopus niveus, an example of unspecific protein catalysis [Internet]. Catalysis Letters. 2017 ; 147( 2): 1977-1987.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10562-017-2121-6
    • Vancouver

      Birolli WG, Fonseca LP, Porto ALM. Aldol reactions by lipase from Rhizopus niveus, an example of unspecific protein catalysis [Internet]. Catalysis Letters. 2017 ; 147( 2): 1977-1987.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10562-017-2121-6
  • Source: Current Microwave Chemistry. Unidade: IQSC

    Assunto: QUÍMICA VERDE

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      JIMENEZ, David Esteban Quintero et al. Silk fibroin functionalized with CuS4O4 on knoevenagel condensation under microwave radiation. Current Microwave Chemistry, v. 20, p. xx-xx, 2017Tradução . . Disponível em: https://doi.org/10.2174/2213335603666160809121421. Acesso em: 24 ago. 2024.
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      Jimenez, D. E. Q., Ferreira, I. M., Yoshioka, S. A., Fonseca, L. P., & Porto, A. L. M. (2017). Silk fibroin functionalized with CuS4O4 on knoevenagel condensation under microwave radiation. Current Microwave Chemistry, 20, xx-xx. doi:10.2174/2213335603666160809121421
    • NLM

      Jimenez DEQ, Ferreira IM, Yoshioka SA, Fonseca LP, Porto ALM. Silk fibroin functionalized with CuS4O4 on knoevenagel condensation under microwave radiation [Internet]. Current Microwave Chemistry. 2017 ; 20 xx-xx.[citado 2024 ago. 24 ] Available from: https://doi.org/10.2174/2213335603666160809121421
    • Vancouver

      Jimenez DEQ, Ferreira IM, Yoshioka SA, Fonseca LP, Porto ALM. Silk fibroin functionalized with CuS4O4 on knoevenagel condensation under microwave radiation [Internet]. Current Microwave Chemistry. 2017 ; 20 xx-xx.[citado 2024 ago. 24 ] Available from: https://doi.org/10.2174/2213335603666160809121421
  • Source: Current Microwave Chemistry. Unidade: IQSC

    Subjects: BENZENO, QUÍMICA ORGÂNICA

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      MEIRELLES, Matheus Andrade et al. Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation. Current Microwave Chemistry, v. 4, p. 1-4 + supl. 1-17, 2017Tradução . . Disponível em: https://doi.org/10.2174/2213335603666161101152243. Acesso em: 24 ago. 2024.
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      Meirelles, M. A., Jeller, A. H., Ferreira, I. M., Raminelli, C., Faria, R. S., Silveira-Lacerda, E. de P., & Porto, A. L. M. (2017). Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation. Current Microwave Chemistry, 4, 1-4 + supl. 1-17. doi:10.2174/2213335603666161101152243
    • NLM

      Meirelles MA, Jeller AH, Ferreira IM, Raminelli C, Faria RS, Silveira-Lacerda E de P, Porto ALM. Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation [Internet]. Current Microwave Chemistry. 2017 ; 4 1-4 + supl. 1-17.[citado 2024 ago. 24 ] Available from: https://doi.org/10.2174/2213335603666161101152243
    • Vancouver

      Meirelles MA, Jeller AH, Ferreira IM, Raminelli C, Faria RS, Silveira-Lacerda E de P, Porto ALM. Biocatalytic production of chiral benzotriazoles employing conventional heating and microwave radiation [Internet]. Current Microwave Chemistry. 2017 ; 4 1-4 + supl. 1-17.[citado 2024 ago. 24 ] Available from: https://doi.org/10.2174/2213335603666161101152243
  • Source: Catalysis Letters. Unidade: IQSC

    Subjects: BIOPOLÍMEROS, BIODIESEL

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      FERREIRA , Irlon Maciel et al. Ethylic biodiesel production using lipase immobilized in silk fibroin-alginate spheres by encapsulation. Catalysis Letters, v. 147, n. 1, p. 269-280, 2017Tradução . . Disponível em: https://doi.org/10.1007/s10562-016-1917-0. Acesso em: 24 ago. 2024.
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      Ferreira , I. M., Ganzeli, L. de S., Rosset, I. G., Yoshioka, S. A., & Porto, A. L. M. (2017). Ethylic biodiesel production using lipase immobilized in silk fibroin-alginate spheres by encapsulation. Catalysis Letters, 147( 1), 269-280. doi:10.1007/s10562-016-1917-0
    • NLM

      Ferreira IM, Ganzeli L de S, Rosset IG, Yoshioka SA, Porto ALM. Ethylic biodiesel production using lipase immobilized in silk fibroin-alginate spheres by encapsulation [Internet]. Catalysis Letters. 2017 ; 147( 1): 269-280.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10562-016-1917-0
    • Vancouver

      Ferreira IM, Ganzeli L de S, Rosset IG, Yoshioka SA, Porto ALM. Ethylic biodiesel production using lipase immobilized in silk fibroin-alginate spheres by encapsulation [Internet]. Catalysis Letters. 2017 ; 147( 1): 269-280.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10562-016-1917-0
  • 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: 24 ago. 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 ago. 24 ] 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 ago. 24 ] Available from: https://doi.org/10.1016/j.molcatb.2016.01.002
  • Source: Marine Biotechnology. Unidade: IQSC

    Assunto: BIODEGRADAÇÃO

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      BIROLLI, Willian Garcia et al. Biodegradation of the pyrethroid pesticide esfenvalerate by marine-derived fungi. Marine Biotechnology, v. 18, n. 4, p. 511-520, 2016Tradução . . Disponível em: https://doi.org/10.1007/s10126-016-9710-z. Acesso em: 24 ago. 2024.
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      Birolli, W. G., Alvarenga, N., Seleghim, M. H. R., & Porto, A. L. M. (2016). Biodegradation of the pyrethroid pesticide esfenvalerate by marine-derived fungi. Marine Biotechnology, 18( 4), 511-520. doi:10.1007/s10126-016-9710-z
    • NLM

      Birolli WG, Alvarenga N, Seleghim MHR, Porto ALM. Biodegradation of the pyrethroid pesticide esfenvalerate by marine-derived fungi [Internet]. Marine Biotechnology. 2016 ; 18( 4): 511-520.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-016-9710-z
    • Vancouver

      Birolli WG, Alvarenga N, Seleghim MHR, Porto ALM. Biodegradation of the pyrethroid pesticide esfenvalerate by marine-derived fungi [Internet]. Marine Biotechnology. 2016 ; 18( 4): 511-520.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s10126-016-9710-z
  • Source: New Biotechnology. Conference titles: European Congress on Biotechnology. Unidade: IQSC

    Assunto: FUNGOS

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      JIMENEZ, David Esteban Quintero e PORTO, Andre Luiz Meleiro. Synthesis one pot of tetrazole-compounds from knoevenaget aducts and one reduction by marine-derived fungus Penicillium citrinun CBMAI 1186. New Biotechnology. Amsterdam: Elsevier. Disponível em: https://doi.org/10.1016/j.nbt.2016.06.068. Acesso em: 24 ago. 2024. , 2016
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      Jimenez, D. E. Q., & Porto, A. L. M. (2016). Synthesis one pot of tetrazole-compounds from knoevenaget aducts and one reduction by marine-derived fungus Penicillium citrinun CBMAI 1186. New Biotechnology. Amsterdam: Elsevier. doi:10.1016/j.nbt.2016.06.068
    • NLM

      Jimenez DEQ, Porto ALM. Synthesis one pot of tetrazole-compounds from knoevenaget aducts and one reduction by marine-derived fungus Penicillium citrinun CBMAI 1186 [Internet]. New Biotechnology. 2016 ; 335[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.nbt.2016.06.068
    • Vancouver

      Jimenez DEQ, Porto ALM. Synthesis one pot of tetrazole-compounds from knoevenaget aducts and one reduction by marine-derived fungus Penicillium citrinun CBMAI 1186 [Internet]. New Biotechnology. 2016 ; 335[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.nbt.2016.06.068

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