Filtros : "Santos Júnior, Fernando M. dos" Limpar

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  • Source: Chirality. Unidade: IQSC

    Assunto: CATÁLISE

    PrivadoAcesso à fonteDOIHow to cite
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    • ABNT

      JIMENEZ, David et al. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, v. 31, p. 534-542, 2019Tradução . . Disponível em: https://doi.org/10.1002/chir.23078. Acesso em: 02 maio 2024.
    • APA

      Jimenez, D., Barreiro, J. C., Santos Júnior, F. M. dos, Vasconcellos, S., Vasconcellos, S. P. de, Porto, A. L. M., & Batista Junior, F. M. (2019). Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra. Chirality, 31, 534-542. doi:10.1002/chir.23078
    • NLM

      Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 maio 02 ] Available from: https://doi.org/10.1002/chir.23078
    • Vancouver

      Jimenez D, Barreiro JC, Santos Júnior FM dos, Vasconcellos S, Vasconcellos SP de, Porto ALM, Batista Junior FM. Enantioselective ene‐reduction of E‐2‐cyano‐3‐(furan‐2‐yl) acrylamide by marine and terrestrial fungi and absolute configuration of (R)‐2‐cyano‐3‐(furan‐2‐yl) propanamide determined by calculations of electronic circular dichroism (ECD) spectra [Internet]. Chirality. 2019 ; 31 534-542.[citado 2024 maio 02 ] Available from: https://doi.org/10.1002/chir.23078
  • Source: Tetrahedron: Asymmetry. Unidade: FCFRP

    Subjects: COMPOSITAE, ANTIOXIDANTES, ANTI-INFLAMATÓRIOS, PRODUTOS NATURAIS, COMPOSTOS FENÓLICOS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      CCANA-CCAPATINTA, Gari V. et al. Absolute configuration assignment of caffeic acid ester derivatives from Tithonia diversifolia by vibrational circular dichroism: the pitfalls of deuteration. Tetrahedron: Asymmetry, v. 28, n. 12, p. 1823-1828, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2017.10.025. Acesso em: 02 maio 2024.
    • APA

      Ccana-Ccapatinta, G. V., Sampaio, B. L., Santos Júnior, F. M. dos, Batista Júnior, J. M., & Costa, F. B. da. (2017). Absolute configuration assignment of caffeic acid ester derivatives from Tithonia diversifolia by vibrational circular dichroism: the pitfalls of deuteration. Tetrahedron: Asymmetry, 28( 12), 1823-1828. doi:10.1016/j.tetasy.2017.10.025
    • NLM

      Ccana-Ccapatinta GV, Sampaio BL, Santos Júnior FM dos, Batista Júnior JM, Costa FB da. Absolute configuration assignment of caffeic acid ester derivatives from Tithonia diversifolia by vibrational circular dichroism: the pitfalls of deuteration [Internet]. Tetrahedron: Asymmetry. 2017 ; 28( 12): 1823-1828.[citado 2024 maio 02 ] Available from: https://doi.org/10.1016/j.tetasy.2017.10.025
    • Vancouver

      Ccana-Ccapatinta GV, Sampaio BL, Santos Júnior FM dos, Batista Júnior JM, Costa FB da. Absolute configuration assignment of caffeic acid ester derivatives from Tithonia diversifolia by vibrational circular dichroism: the pitfalls of deuteration [Internet]. Tetrahedron: Asymmetry. 2017 ; 28( 12): 1823-1828.[citado 2024 maio 02 ] Available from: https://doi.org/10.1016/j.tetasy.2017.10.025

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