Filtros : "Balfour, Michael N" Limpar

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  • Source: Tetrahedron. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
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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: 23 maio 2024.
    • APA

      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 23 ] 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 23 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
  • Source: Synthetic Communications. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, SÍNTESE QUÍMICA

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    • ABNT

      BALFOUR, Michael N et al. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, v. 49, n. 3, p. 351-358, 2019Tradução . . Disponível em: https://doi.org/10.1080/00397911.2018.1545032. Acesso em: 23 maio 2024.
    • APA

      Balfour, M. N., Schpector, J. Z., Rodriguez, M. J. D., Reis, J. S. dos, Esteves, C. H. A., & Stefani, H. A. (2019). Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, 49( 3), 351-358. doi:10.1080/00397911.2018.1545032
    • NLM

      Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 maio 23 ] Available from: https://doi.org/10.1080/00397911.2018.1545032
    • Vancouver

      Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 maio 23 ] Available from: https://doi.org/10.1080/00397911.2018.1545032
  • Source: European Journal of Medicinal Chemistry. Unidade: FCF

    Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA

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    • ABNT

      BALFOUR, Michael N et al. Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols. European Journal of Medicinal Chemistry, v. 128, p. 202-212, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.01.040. Acesso em: 23 maio 2024.
    • APA

      Balfour, M. N., Franco, C. H., Moraes, C. B., Freitas Junior, L. H., & Stefani, H. A. (2017). Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols. European Journal of Medicinal Chemistry, 128, 202-212. doi:10.1016/j.ejmech.2017.01.040
    • NLM

      Balfour MN, Franco CH, Moraes CB, Freitas Junior LH, Stefani HA. Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols [Internet]. European Journal of Medicinal Chemistry. 2017 ; 128 202-212.[citado 2024 maio 23 ] Available from: https://doi.org/10.1016/j.ejmech.2017.01.040
    • Vancouver

      Balfour MN, Franco CH, Moraes CB, Freitas Junior LH, Stefani HA. Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols [Internet]. European Journal of Medicinal Chemistry. 2017 ; 128 202-212.[citado 2024 maio 23 ] Available from: https://doi.org/10.1016/j.ejmech.2017.01.040

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