Filtros : "Oliveira, Isadora M. de" Limpar

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  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: ANTINEOPLÁSICOS, ANTIPROTOZOÁRIOS, APOPTOSE

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    • ABNT

      COSTA, Claudia A et al. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, v. 28, p. 1-13 art. 115511, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115511. Acesso em: 29 maio 2024.
    • APA

      Costa, C. A., Lopes, R. M., Ferraz, L. S., Esteves, G. N. N., Di Iorio, J. F., Souza, A. A., et al. (2020). Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, 28, 1-13 art. 115511. doi:10.1016/j.bmc.2020.115511
    • NLM

      Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
    • Vancouver

      Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
  • Source: Tetrahedron. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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    • ABNT

      VASCONCELOS, Stanley N. S et al. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, v. 75, p. 1865-1959, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2019.02.001. Acesso em: 29 maio 2024.
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      Vasconcelos, S. N. S., Reis, J. S., Oliveira, I. M. de, Balfour, M. N., & Stefani, H. A. (2019). Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, 75, 1865-1959. doi:10.1016/j.tet.2019.02.001
    • NLM

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
    • Vancouver

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
  • Source: RSC Advances. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      DARBEM, Mariana P et al. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, v. 9, p. 9468–9474, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9ra00523d. Acesso em: 29 maio 2024.
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      Darbem, M. P., Esteves, C. H. A., Oliveira, I. M. de, Reis, J. S., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, 9, 9468–9474. doi:10.1039/c9ra00523d
    • NLM

      Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c9ra00523d
    • Vancouver

      Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c9ra00523d
  • Source: New Journal of Chemistry. Unidade: FCF

    Subjects: MONÓXIDO DE CARBONO, MOLIBDÊNIO

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    • ABNT

      DARBEM, Mariana P et al. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, v. 43, n. 2, p. 696-699, 2019Tradução . . Disponível em: https://doi.org/10.1039/c8nj04540b. Acesso em: 29 maio 2024.
    • APA

      Darbem, M. P., Kanno, K. S., Oliveira, I. M. de, Esteves, C. H. A., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, 43( 2), 696-699. doi:10.1039/c8nj04540b
    • NLM

      Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c8nj04540b
    • Vancouver

      Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c8nj04540b
  • Source: Advanced Synthesis and Catalysis. Unidade: FCF

    Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO

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    • ABNT

      OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 29 maio 2024.
    • APA

      Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142
    • NLM

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/adsc.201900142
    • Vancouver

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/adsc.201900142
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ITÉRBIO, SÍNTESE ORGÂNICA

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    • ABNT

      OLIVEIRA, Isadora M. de et al. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, v. 59, n. 24, p. 3907-3911, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.09.022. Acesso em: 29 maio 2024.
    • APA

      Oliveira, I. M. de, Darbem, M. P., Esteves, C. H. A., Pimenta, D. C., Schpector, J. Z., Stefani, H. A., & Manarin, F. (2018). Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, 59( 24), 3907-3911. doi:10.1016/j.tetlet.2018.09.022
    • NLM

      Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
    • Vancouver

      Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
  • Source: New Journal of Chemistry. Unidades: IQ, FCF

    Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS

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      OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 29 maio 2024.
    • APA

      Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g
    • NLM

      Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c7nj01803g
    • Vancouver

      Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c7nj01803g
  • Source: Molecular Diversity. Unidade: FCF

    Subjects: PEPTÍDEOS, TIROXINA

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      VASCONCELOS, Stanley Nunes Siqueira et al. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, v. 20, n. 2, p. 469-481, 2016Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9642-y. Acesso em: 29 maio 2024.
    • APA

      Vasconcelos, S. N. S., Shamim, A., Ali, B., Oliveira, I. M. de, & Stefani, H. A. (2016). Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine. Molecular Diversity, 20( 2), 469-481. doi:10.1007/s11030-015-9642-y
    • NLM

      Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 maio 29 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
    • Vancouver

      Vasconcelos SNS, Shamim A, Ali B, Oliveira IM de, Stefani HA. Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine [Internet]. Molecular Diversity. 2016 ; 20( 2): 469-481.[citado 2024 maio 29 ] Available from: https://doi.org/10.1007/s11030-015-9642-y

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