Filtros : "Cross coupling reaction" Limpar

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  • Source: The Journal of Physical Chemistry Part C. Unidade: IQSC

    Subjects: CATÁLISE, FLUORESCÊNCIA, PALÁDIO

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    • ABNT

      REIS, Izadora F. e GEHLEN, Marcelo Henrique. Exploring the dynamics of Suzuki−Miyaura cross-coupling reactions via single-molecule fluorescence microscopy: Catalytic efficiency from SM-TOF measurements. The Journal of Physical Chemistry Part C, v. 129, n. 8, p. 4052-4058, 2025Tradução . . Disponível em: https://doi.org/10.1021/acs.jpcc.4c07269. Acesso em: 22 abr. 2026.
    • APA

      Reis, I. F., & Gehlen, M. H. (2025). Exploring the dynamics of Suzuki−Miyaura cross-coupling reactions via single-molecule fluorescence microscopy: Catalytic efficiency from SM-TOF measurements. The Journal of Physical Chemistry Part C, 129( 8), 4052-4058. doi:10.1021/acs.jpcc.4c07269
    • NLM

      Reis IF, Gehlen MH. Exploring the dynamics of Suzuki−Miyaura cross-coupling reactions via single-molecule fluorescence microscopy: Catalytic efficiency from SM-TOF measurements [Internet]. The Journal of Physical Chemistry Part C. 2025 ; 129( 8): 4052-4058.[citado 2026 abr. 22 ] Available from: https://doi.org/10.1021/acs.jpcc.4c07269
    • Vancouver

      Reis IF, Gehlen MH. Exploring the dynamics of Suzuki−Miyaura cross-coupling reactions via single-molecule fluorescence microscopy: Catalytic efficiency from SM-TOF measurements [Internet]. The Journal of Physical Chemistry Part C. 2025 ; 129( 8): 4052-4058.[citado 2026 abr. 22 ] Available from: https://doi.org/10.1021/acs.jpcc.4c07269
  • Source: The Journal of Physical Chemistry Letters. Unidade: IQSC

    Subjects: CATALISADORES, FLUORESCÊNCIA, PALÁDIO

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    • ABNT

      REIS, Izadora F. e GEHLEN, Marcelo Henrique. Single-Molecule Catalysis in the Palladium Cross-Coupling Reaction Cycle. The Journal of Physical Chemistry Letters, v. 15, n. 9, p. 2352–2358, 2024Tradução . . Disponível em: https://doi.org/10.1021/acs.jpclett.3c03623. Acesso em: 22 abr. 2026.
    • APA

      Reis, I. F., & Gehlen, M. H. (2024). Single-Molecule Catalysis in the Palladium Cross-Coupling Reaction Cycle. The Journal of Physical Chemistry Letters, 15( 9), 2352–2358. doi:10.1021/acs.jpclett.3c03623
    • NLM

      Reis IF, Gehlen MH. Single-Molecule Catalysis in the Palladium Cross-Coupling Reaction Cycle [Internet]. The Journal of Physical Chemistry Letters. 2024 ;15( 9): 2352–2358.[citado 2026 abr. 22 ] Available from: https://doi.org/10.1021/acs.jpclett.3c03623
    • Vancouver

      Reis IF, Gehlen MH. Single-Molecule Catalysis in the Palladium Cross-Coupling Reaction Cycle [Internet]. The Journal of Physical Chemistry Letters. 2024 ;15( 9): 2352–2358.[citado 2026 abr. 22 ] Available from: https://doi.org/10.1021/acs.jpclett.3c03623
  • Source: Organic Letters. Unidades: FFCLRP, FCFRP

    Subjects: COMPOSTOS DE NITROGÊNIO, NITRILAS, QUÍMICA ORGÂNICA, COMPOSTOS HETEROCÍCLICOS

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    • ABNT

      SANTOS, Thiago dos et al. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, v. 23, n. 19, p. 7396-7400, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c02572. Acesso em: 22 abr. 2026.
    • APA

      Santos, T. dos, Orenha, H. P., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2021). Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, 23( 19), 7396-7400. doi:10.1021/acs.orglett.1c02572
    • NLM

      Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2026 abr. 22 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
    • Vancouver

      Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2026 abr. 22 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572

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