Filtros : "BERCI FILHO, PEDRO" "Indexado no Chemistry Citation Index" Removido: " IFSC033" Limpar

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  • Source: Journal of Physical Organic Chemistry. Unidades: IQSC, IQ

    Assunto: FÍSICO-QUÍMICA ORGÂNICA

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

      TRIBONI, Eduardo Rezende et al. Aromatic nitro substitution reaction between 4-nitro-N-n-butyl-1,8-naphthalimide and n-heptanethiol in water-methanol binary mixtures. Journal of Physical Organic Chemistry, v. 22, p. 703-708, 2009Tradução . . Disponível em: https://doi.org/10.1002/poc.1504. Acesso em: 19 ago. 2024.
    • APA

      Triboni, E. R., Artur, J. C., Berci Filho, P., Cuccovia, I. M., & Politi, M. J. (2009). Aromatic nitro substitution reaction between 4-nitro-N-n-butyl-1,8-naphthalimide and n-heptanethiol in water-methanol binary mixtures. Journal of Physical Organic Chemistry, 22, 703-708. doi:10.1002/poc.1504
    • NLM

      Triboni ER, Artur JC, Berci Filho P, Cuccovia IM, Politi MJ. Aromatic nitro substitution reaction between 4-nitro-N-n-butyl-1,8-naphthalimide and n-heptanethiol in water-methanol binary mixtures [Internet]. Journal of Physical Organic Chemistry. 2009 ; 22 703-708.[citado 2024 ago. 19 ] Available from: https://doi.org/10.1002/poc.1504
    • Vancouver

      Triboni ER, Artur JC, Berci Filho P, Cuccovia IM, Politi MJ. Aromatic nitro substitution reaction between 4-nitro-N-n-butyl-1,8-naphthalimide and n-heptanethiol in water-methanol binary mixtures [Internet]. Journal of Physical Organic Chemistry. 2009 ; 22 703-708.[citado 2024 ago. 19 ] Available from: https://doi.org/10.1002/poc.1504
  • Source: Journal of Physical Organic Chemistry. Unidades: IQ, IQSC

    Assunto: FÍSICO-QUÍMICA ORGÂNICA

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

      TRIBONI, Eduardo Rezende et al. Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide. Journal of Physical Organic Chemistry, v. 16, p. 311-317, 2003Tradução . . Disponível em: https://doi.org/10.1002/poc.618. Acesso em: 19 ago. 2024.
    • APA

      Triboni, E. R., Politi, M. J., Cuccovia, I. M., Chaimovich Guralnik, H., & Berci Filho, P. (2003). Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide. Journal of Physical Organic Chemistry, 16, 311-317. doi:10.1002/poc.618
    • NLM

      Triboni ER, Politi MJ, Cuccovia IM, Chaimovich Guralnik H, Berci Filho P. Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide [Internet]. Journal of Physical Organic Chemistry. 2003 ; 16 311-317.[citado 2024 ago. 19 ] Available from: https://doi.org/10.1002/poc.618
    • Vancouver

      Triboni ER, Politi MJ, Cuccovia IM, Chaimovich Guralnik H, Berci Filho P. Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide [Internet]. Journal of Physical Organic Chemistry. 2003 ; 16 311-317.[citado 2024 ago. 19 ] Available from: https://doi.org/10.1002/poc.618

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