Filtros : "STEFANI, HELIO ALEXANDRE" "Ali, Bakhat" Limpar

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  • Source: Journal of Fluorescence. Unidades: FCF, IPEN

    Subjects: LUMINESCÊNCIA, EURÓPIO, TÉRBIO

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    • ABNT

      ALI, Bakhat et al. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes. Journal of Fluorescence, v. 30, p. 1345–1355, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10895-020-02613-z. Acesso em: 11 nov. 2024.
    • APA

      Ali, B., Stefani, H. A., Imran, M., Irfan, A., Assiri, M. A., Felinto, M. C. F. da C., et al. (2020). Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes. Journal of Fluorescence, 30, 1345–1355. doi:10.1007/s10895-020-02613-z
    • NLM

      Ali B, Stefani HA, Imran M, Irfan A, Assiri MA, Felinto MCF da C, Khalid M, Al-Sehemi AG. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes [Internet]. Journal of Fluorescence. 2020 ; 30 1345–1355.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10895-020-02613-z
    • Vancouver

      Ali B, Stefani HA, Imran M, Irfan A, Assiri MA, Felinto MCF da C, Khalid M, Al-Sehemi AG. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes [Internet]. Journal of Fluorescence. 2020 ; 30 1345–1355.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10895-020-02613-z
  • Source: Arabian Journal of Chemistry. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS

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    • ABNT

      ALI, Bakhat et al. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, v. 10, n. 4, p. 500-508, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.06.003. Acesso em: 11 nov. 2024.
    • APA

      Ali, B., Vasconcelos, S. N. S., Shamim, A., Schpector, J. Z., & Stefani, H. A. (2017). Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, 10( 4), 500-508. doi:10.1016/j.arabjc.2016.06.003
    • NLM

      Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
    • Vancouver

      Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
  • Source: Molecular Diversity. Unidade: FCF

    Subjects: PEPTÍDEOS, TIROXINA

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    • ABNT

      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: 11 nov. 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 nov. 11 ] 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 nov. 11 ] Available from: https://doi.org/10.1007/s11030-015-9642-y
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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    • ABNT

      SHAMIM, Anwar et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 11 nov. 2024.
    • APA

      Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052
    • NLM

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
    • Vancouver

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      ALI, Bakhat et al. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, v. 56, n. 28, p. 4234-4241, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.05.066. Acesso em: 11 nov. 2024.
    • APA

      Ali, B., Shamim, A., Vasconcelos, S. N. S., & Stefani, H. A. (2015). Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, 56( 28), 4234-4241. doi:10.1016/j.tetlet.2015.05.066
    • NLM

      Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
    • Vancouver

      Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINAS, CATÁLISE

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    • ABNT

      ALI, Bakhat et al. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, v. 56, n. 9, p. 1153-1158, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 11 nov. 2024.
    • APA

      Ali, B., Schpector, J. Z., Ferreira, F. P., Shamim, A., Pimenta, D. C., & Stefani, H. A. (2015). Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, 56( 9), 1153-1158. doi:10.1016/j.tetlet.2015.01.059
    • NLM

      Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
    • Vancouver

      Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      STEFANI, Hélio Alexandre et al. Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, v. 55, n. 31, p. 4355-4358, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.05.095. Acesso em: 11 nov. 2024.
    • APA

      Stefani, H. A., Ferreira, F. P., Ali, B., & Pimenta, D. C. (2014). Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, 55( 31), 4355-4358. doi:10.1016/j.tetlet.2014.05.095
    • NLM

      Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
    • Vancouver

      Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095

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