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  • Source: Current Microwave Chemistry. Unidades: IFSC, IQSC

    Subjects: TECNOLOGIA DE MICRO-ONDAS, CRISTALOGRAFIA ESTRUTURAL

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    • ABNT

      JIMENEZ, David Esteban Quintero et al. Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation. Current Microwave Chemistry, v. 6, n. 1, p. 54-60, 2019Tradução . . Disponível em: https://doi.org/10.2174/2213335606666190906123431. Acesso em: 08 jun. 2024.
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      Jimenez, D. E. Q., Zanin, L. L., Diniz, L. F., Ellena, J., & Porto, A. L. M. (2019). Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation. Current Microwave Chemistry, 6( 1), 54-60. doi:10.2174/2213335606666190906123431
    • NLM

      Jimenez DEQ, Zanin LL, Diniz LF, Ellena J, Porto ALM. Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation [Internet]. Current Microwave Chemistry. 2019 ; 6( 1): 54-60.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2174/2213335606666190906123431
    • Vancouver

      Jimenez DEQ, Zanin LL, Diniz LF, Ellena J, Porto ALM. Green synthetic methodology of (E)-2-cyano-3-aryl selective knoevenagel adducts under microwave irradiation [Internet]. Current Microwave Chemistry. 2019 ; 6( 1): 54-60.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2174/2213335606666190906123431
  • Source: Current Microwave Chemistry. Unidade: FFCLRP

    Subjects: SÍNTESE ORGÂNICA, PRODUTOS NATURAIS, CYANOPHYTA, RADIAÇÃO ELETROMAGNÉTICA

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      PREVIDI, Daniel e ROSA, Mayla E. e DONATE, Paulo Marcos. Fast and efficient synthesis of maculalactone derivatives via the microwave technique. Current Microwave Chemistry, v. 4, n. 3, p. 229-237, 2017Tradução . . Disponível em: https://doi.org/10.2174/2213335604666170616122835. Acesso em: 08 jun. 2024.
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      Previdi, D., Rosa, M. E., & Donate, P. M. (2017). Fast and efficient synthesis of maculalactone derivatives via the microwave technique. Current Microwave Chemistry, 4( 3), 229-237. doi:10.2174/2213335604666170616122835
    • NLM

      Previdi D, Rosa ME, Donate PM. Fast and efficient synthesis of maculalactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2017 ; 4( 3): 229-237.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2174/2213335604666170616122835
    • Vancouver

      Previdi D, Rosa ME, Donate PM. Fast and efficient synthesis of maculalactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2017 ; 4( 3): 229-237.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2174/2213335604666170616122835
  • 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: 08 jun. 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 jun. 08 ] 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 jun. 08 ] 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: 08 jun. 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 jun. 08 ] 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 jun. 08 ] Available from: https://doi.org/10.2174/2213335603666161101152243
  • Source: Current Microwave Chemistry. Unidade: IQSC

    Assunto: BACTÉRIAS TERMÓFILAS

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      RIBEIRO, Sandra Santos et al. Application of conventional heating and microwave irradiation for the biocatalytic reduction of fluoroacetophenomes by thermophilic bacteria. Current Microwave Chemistry, v. 3, n. 1, p. 9-13, 2016Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/5acb6c66-ea61-42a2-9c57-5615e6b594d1/P16516.pdf. Acesso em: 08 jun. 2024.
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      Ribeiro, S. S., Vasconcellos, S. P. de, Ramos, P. L., Cruz, J. B. da, & Porto, A. L. M. (2016). Application of conventional heating and microwave irradiation for the biocatalytic reduction of fluoroacetophenomes by thermophilic bacteria. Current Microwave Chemistry, 3( 1), 9-13. Recuperado de https://repositorio.usp.br/directbitstream/5acb6c66-ea61-42a2-9c57-5615e6b594d1/P16516.pdf
    • NLM

      Ribeiro SS, Vasconcellos SP de, Ramos PL, Cruz JB da, Porto ALM. Application of conventional heating and microwave irradiation for the biocatalytic reduction of fluoroacetophenomes by thermophilic bacteria [Internet]. Current Microwave Chemistry. 2016 ; 3( 1): 9-13.[citado 2024 jun. 08 ] Available from: https://repositorio.usp.br/directbitstream/5acb6c66-ea61-42a2-9c57-5615e6b594d1/P16516.pdf
    • Vancouver

      Ribeiro SS, Vasconcellos SP de, Ramos PL, Cruz JB da, Porto ALM. Application of conventional heating and microwave irradiation for the biocatalytic reduction of fluoroacetophenomes by thermophilic bacteria [Internet]. Current Microwave Chemistry. 2016 ; 3( 1): 9-13.[citado 2024 jun. 08 ] Available from: https://repositorio.usp.br/directbitstream/5acb6c66-ea61-42a2-9c57-5615e6b594d1/P16516.pdf
  • Source: Current Microwave Chemistry. Unidade: FFCLRP

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, TECNOLOGIA DE MICRO-ONDAS, PRODUTOS NATURAIS

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      PINATTO-BOTELHO, Marcos F e DONATE, Paulo Marcos. A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique. Current Microwave Chemistry, v. 2, n. 1, p. 83-87, 2015Tradução . . Disponível em: https://doi.org/10.2174/221333560201150212113120. Acesso em: 08 jun. 2024.
    • APA

      Pinatto-Botelho, M. F., & Donate, P. M. (2015). A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique. Current Microwave Chemistry, 2( 1), 83-87. doi:10.2174/221333560201150212113120
    • NLM

      Pinatto-Botelho MF, Donate PM. A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2015 ; 2( 1): 83-87.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2174/221333560201150212113120
    • Vancouver

      Pinatto-Botelho MF, Donate PM. A rapid protocol to synthesize γ-butyrolactone derivatives via the microwave technique [Internet]. Current Microwave Chemistry. 2015 ; 2( 1): 83-87.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2174/221333560201150212113120
  • Source: Current Microwave Chemistry. Unidade: IQSC

    Assunto: FUNGOS

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      RIBEIRO, Sandra Santos e SETTE, Lara Durães e PORTO, Andre Luiz Meleiro. First bioreduction of 2,2,2-trifluoro-1-phenylethanone by Whole Hyphae of marine fungus mucor racemosus CBMAI 847 under microwave radiation. Current Microwave Chemistry, v. 2, p. 1-5, 2015Tradução . . Disponível em: https://doi.org/10.2147/22133356026661506222320. Acesso em: 08 jun. 2024.
    • APA

      Ribeiro, S. S., Sette, L. D., & Porto, A. L. M. (2015). First bioreduction of 2,2,2-trifluoro-1-phenylethanone by Whole Hyphae of marine fungus mucor racemosus CBMAI 847 under microwave radiation. Current Microwave Chemistry, 2, 1-5. doi:10.2147/22133356026661506222320
    • NLM

      Ribeiro SS, Sette LD, Porto ALM. First bioreduction of 2,2,2-trifluoro-1-phenylethanone by Whole Hyphae of marine fungus mucor racemosus CBMAI 847 under microwave radiation [Internet]. Current Microwave Chemistry. 2015 ; 2 1-5.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2147/22133356026661506222320
    • Vancouver

      Ribeiro SS, Sette LD, Porto ALM. First bioreduction of 2,2,2-trifluoro-1-phenylethanone by Whole Hyphae of marine fungus mucor racemosus CBMAI 847 under microwave radiation [Internet]. Current Microwave Chemistry. 2015 ; 2 1-5.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2147/22133356026661506222320
  • 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: 08 jun. 2024.
    • APA

      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
    • NLM

      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 jun. 08 ] 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 jun. 08 ] Available from: https://repositorio.usp.br/directbitstream/fcf731d7-5e3f-41c7-979c-a9a5c630747c/P15157.pdf

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