Filtros : "QUÍMICA ORGÂNICA" "Journal of Physical Organic Chemistry" Removido: "Financiamento PIBIC/CNPq-PIC/PRPI/USP" Limpar

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

    Subjects: SOLVENTE, QUÍMICA ORGÂNICA, FÍSICA

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    • ABNT

      PIRES, Paulo A. R. et al. Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability. Journal of Physical Organic Chemistry, v. 26, n. 3, p. 280-285, 2013Tradução . . Disponível em: https://doi.org/10.1002/poc.3083. Acesso em: 11 dez. 2025.
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      Pires, P. A. R., Imran, M., Loffredo, C., Donate, P. M., Previdi, D., & El Seoud, O. A. (2013). Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability. Journal of Physical Organic Chemistry, 26( 3), 280-285. doi:10.1002/poc.3083
    • NLM

      Pires PAR, Imran M, Loffredo C, Donate PM, Previdi D, El Seoud OA. Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability [Internet]. Journal of Physical Organic Chemistry. 2013 ; 26( 3): 280-285.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.3083
    • Vancouver

      Pires PAR, Imran M, Loffredo C, Donate PM, Previdi D, El Seoud OA. Solvatochromism of 2-(N,N-dimethylamino)-7-nitrofluorene and the natural dye 'beta'-carotene: application for the determination of solvent dipolarity and polarizability [Internet]. Journal of Physical Organic Chemistry. 2013 ; 26( 3): 280-285.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.3083
  • Source: Journal of Physical Organic Chemistry. Unidade: IFSC

    Subjects: REAÇÕES QUÍMICAS, QUÍMICA ORGÂNICA, CRISTALOGRAFIA

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      CARAM, José Alberto et al. Reactions of the activated, rigid, 'ALFA'-diazomethine group of 1,2,5-thiadiazole 1,1-dioxes with nitrogenated nucleophiles. Part III: aliphatic monoamines and phenylhydrazine. Journal of Physical Organic Chemistry, v. 19, n. 4, p. 229-237, 2006Tradução . . Disponível em: https://doi.org/10.1002/poc.1022. Acesso em: 11 dez. 2025.
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      Caram, J. A., Piro, O. E., Castellano, E. E., Mirífico, M. V., & Vasini, E. J. (2006). Reactions of the activated, rigid, 'ALFA'-diazomethine group of 1,2,5-thiadiazole 1,1-dioxes with nitrogenated nucleophiles. Part III: aliphatic monoamines and phenylhydrazine. Journal of Physical Organic Chemistry, 19( 4), 229-237. doi:10.1002/poc.1022
    • NLM

      Caram JA, Piro OE, Castellano EE, Mirífico MV, Vasini EJ. Reactions of the activated, rigid, 'ALFA'-diazomethine group of 1,2,5-thiadiazole 1,1-dioxes with nitrogenated nucleophiles. Part III: aliphatic monoamines and phenylhydrazine [Internet]. Journal of Physical Organic Chemistry. 2006 ; 19( 4): 229-237.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.1022
    • Vancouver

      Caram JA, Piro OE, Castellano EE, Mirífico MV, Vasini EJ. Reactions of the activated, rigid, 'ALFA'-diazomethine group of 1,2,5-thiadiazole 1,1-dioxes with nitrogenated nucleophiles. Part III: aliphatic monoamines and phenylhydrazine [Internet]. Journal of Physical Organic Chemistry. 2006 ; 19( 4): 229-237.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.1022
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      BLAGOEVA, Iva B. et al. Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis. Journal of Physical Organic Chemistry, v. 18, n. 8, p. 850-855, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.953. Acesso em: 11 dez. 2025.
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      Blagoeva, I. B., Ouarti, N., El Seoud, O. A., & Ruasse, M. -F. (2005). Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis. Journal of Physical Organic Chemistry, 18( 8), 850-855. doi:10.1002/poc.953
    • NLM

      Blagoeva IB, Ouarti N, El Seoud OA, Ruasse M-F. Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 8): 850-855.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.953
    • Vancouver

      Blagoeva IB, Ouarti N, El Seoud OA, Ruasse M-F. Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 8): 850-855.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.953
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: ÁLCOOL, QUÍMICA ORGÂNICA

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      TADA, Erika Batista e SILVA, Priscilla Leandro e EL SEOUD, Omar A. Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions. Journal of Physical Organic Chemistry, v. 18, n. 5, p. 398-407, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.887. Acesso em: 11 dez. 2025.
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      Tada, E. B., Silva, P. L., & El Seoud, O. A. (2005). Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions. Journal of Physical Organic Chemistry, 18( 5), 398-407. doi:10.1002/poc.887
    • NLM

      Tada EB, Silva PL, El Seoud OA. Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 5): 398-407.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.887
    • Vancouver

      Tada EB, Silva PL, El Seoud OA. Thermo-solvatochromism of zwitterionic probes in aqueous aliphatic alcohols and in aqueous 2-alkoxyethanols: relevance to the enthalpies of activation of chemical reactions [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 5): 398-407.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.887
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: HIDRÓLISE, QUÍMICA ORGÂNICA

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      EL SEOUD, Omar A et al. Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group. Journal of Physical Organic Chemistry, v. 18, n. 2, p. 173-182, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.864. Acesso em: 11 dez. 2025.
    • APA

      El Seoud, O. A., Ferreira, M., Rodrigues, W. A., & Ruasse, M. -F. (2005). Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group. Journal of Physical Organic Chemistry, 18( 2), 173-182. doi:10.1002/poc.864
    • NLM

      El Seoud OA, Ferreira M, Rodrigues WA, Ruasse M-F. Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 2): 173-182.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.864
    • Vancouver

      El Seoud OA, Ferreira M, Rodrigues WA, Ruasse M-F. Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 2): 173-182.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.864
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SOLVENTE, FÍSICO-QUÍMICA

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      MARTINS, Clarissa T. e LIMA, Michelle de Souza e EL SEOUD, Omar A. A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle. Journal of Physical Organic Chemistry, v. 18, n. 11, p. 1072-1085, 2005Tradução . . Disponível em: https://doi.org/10.1002/poc.975. Acesso em: 11 dez. 2025.
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      Martins, C. T., Lima, M. de S., & El Seoud, O. A. (2005). A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle. Journal of Physical Organic Chemistry, 18( 11), 1072-1085. doi:10.1002/poc.975
    • NLM

      Martins CT, Lima M de S, El Seoud OA. A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 11): 1072-1085.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.975
    • Vancouver

      Martins CT, Lima M de S, El Seoud OA. A novel, convenient, quinoline-based merocyanine dye: probing solvation in pure and mixed solvents and in the interfacial region of an anionic micelle [Internet]. Journal of Physical Organic Chemistry. 2005 ; 18( 11): 1072-1085.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.975
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, ANÁLISE ESPECTROQUÍMICA, ÁLCOOL, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)

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      ANTONIOUS, Maged S. e TADA, Erika Batista e EL SEOUD, Omar A. Thermo-solvatochromism in aqueous alcohols: effects of the molecular structures of the alcohol and the solvatochromic probe. Journal of Physical Organic Chemistry, v. 15, n. 7, p. 403-412, 2002Tradução . . Disponível em: https://doi.org/10.1002/poc.510. Acesso em: 11 dez. 2025.
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      Antonious, M. S., Tada, E. B., & El Seoud, O. A. (2002). Thermo-solvatochromism in aqueous alcohols: effects of the molecular structures of the alcohol and the solvatochromic probe. Journal of Physical Organic Chemistry, 15( 7), 403-412. doi:10.1002/poc.510
    • NLM

      Antonious MS, Tada EB, El Seoud OA. Thermo-solvatochromism in aqueous alcohols: effects of the molecular structures of the alcohol and the solvatochromic probe [Internet]. Journal of Physical Organic Chemistry. 2002 ; 15( 7): 403-412.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.510
    • Vancouver

      Antonious MS, Tada EB, El Seoud OA. Thermo-solvatochromism in aqueous alcohols: effects of the molecular structures of the alcohol and the solvatochromic probe [Internet]. Journal of Physical Organic Chemistry. 2002 ; 15( 7): 403-412.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.510
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SOLUÇÕES AQUOSAS, SURFACTANTES

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      OUARTI, Nadia et al. Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8. Journal of Physical Organic Chemistry, v. 14, n. 11, p. 823-831, 2001Tradução . . Disponível em: https://doi.org/10.1002/poc.441.abs. Acesso em: 11 dez. 2025.
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      Ouarti, N., Blagoeva, I. B., El Seoud, O. A., & Ruasse, M. -F. (2001). Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8. Journal of Physical Organic Chemistry, 14( 11), 823-831. doi:10.1002/poc.441.abs
    • NLM

      Ouarti N, Blagoeva IB, El Seoud OA, Ruasse M-F. Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8 [Internet]. Journal of Physical Organic Chemistry. 2001 ; 14( 11): 823-831.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.441.abs
    • Vancouver

      Ouarti N, Blagoeva IB, El Seoud OA, Ruasse M-F. Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7-8 [Internet]. Journal of Physical Organic Chemistry. 2001 ; 14( 11): 823-831.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.441.abs
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      TADA, Erika Batista e NOVAKI, Luzia Peres e EL SEOUD, Omar A. Solvatochromism in pure and binary solvent mixtures: effects of the molecular structure of the zwitterionic probe. Journal of Physical Organic Chemistry, v. 13, n. 11, p. 679-687, 2000Tradução . . Disponível em: https://doi.org/10.1002/1099-1395(200011)13:11%3C679::aid-poc299%3E3.0.co;2-r. Acesso em: 11 dez. 2025.
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      Tada, E. B., Novaki, L. P., & El Seoud, O. A. (2000). Solvatochromism in pure and binary solvent mixtures: effects of the molecular structure of the zwitterionic probe. Journal of Physical Organic Chemistry, 13( 11), 679-687. doi:10.1002/1099-1395(200011)13:11%3C679::aid-poc299%3E3.0.co;2-r
    • NLM

      Tada EB, Novaki LP, El Seoud OA. Solvatochromism in pure and binary solvent mixtures: effects of the molecular structure of the zwitterionic probe [Internet]. Journal of Physical Organic Chemistry. 2000 ; 13( 11): 679-687.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/1099-1395(200011)13:11%3C679::aid-poc299%3E3.0.co;2-r
    • Vancouver

      Tada EB, Novaki LP, El Seoud OA. Solvatochromism in pure and binary solvent mixtures: effects of the molecular structure of the zwitterionic probe [Internet]. Journal of Physical Organic Chemistry. 2000 ; 13( 11): 679-687.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/1099-1395(200011)13:11%3C679::aid-poc299%3E3.0.co;2-r
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, HIDRÓLISE

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      POSSIDONIO, Shirley e SIVIERO, Fábio e EL SEOUD, Omar A. Kinetics of the pH-independent hydrolysis of 4-nitrophenyl chloroformate in aqueous micellar solutions: effects of the charge and structure of the surfactant. Journal of Physical Organic Chemistry, v. 12, n. 4, p. 325-332, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1099-1395(199904)12:4%3C325::aid-poc136%3E3.0.co;2-i. Acesso em: 11 dez. 2025.
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      Possidonio, S., Siviero, F., & El Seoud, O. A. (1999). Kinetics of the pH-independent hydrolysis of 4-nitrophenyl chloroformate in aqueous micellar solutions: effects of the charge and structure of the surfactant. Journal of Physical Organic Chemistry, 12( 4), 325-332. doi:10.1002/(sici)1099-1395(199904)12:4%3C325::aid-poc136%3E3.0.co;2-i
    • NLM

      Possidonio S, Siviero F, El Seoud OA. Kinetics of the pH-independent hydrolysis of 4-nitrophenyl chloroformate in aqueous micellar solutions: effects of the charge and structure of the surfactant [Internet]. Journal of Physical Organic Chemistry. 1999 ; 12( 4): 325-332.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/(sici)1099-1395(199904)12:4%3C325::aid-poc136%3E3.0.co;2-i
    • Vancouver

      Possidonio S, Siviero F, El Seoud OA. Kinetics of the pH-independent hydrolysis of 4-nitrophenyl chloroformate in aqueous micellar solutions: effects of the charge and structure of the surfactant [Internet]. Journal of Physical Organic Chemistry. 1999 ; 12( 4): 325-332.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/(sici)1099-1395(199904)12:4%3C325::aid-poc136%3E3.0.co;2-i
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      STEVANI, Cassius Vinicius e BAADER, Wilhelm Josef. Kinetic studies on the chemiluminescent decomposition of an isolated intermediatin the peroxyoxylate reaction. Journal of Physical Organic Chemistry, v. 10, n. 8, p. 593-599, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1099-1395(199708)10:8%3C593::aid-poc926%3E3.0.co;2-h. Acesso em: 11 dez. 2025.
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      Stevani, C. V., & Baader, W. J. (1997). Kinetic studies on the chemiluminescent decomposition of an isolated intermediatin the peroxyoxylate reaction. Journal of Physical Organic Chemistry, 10( 8), 593-599. doi:10.1002/(sici)1099-1395(199708)10:8%3C593::aid-poc926%3E3.0.co;2-h
    • NLM

      Stevani CV, Baader WJ. Kinetic studies on the chemiluminescent decomposition of an isolated intermediatin the peroxyoxylate reaction [Internet]. Journal of Physical Organic Chemistry. 1997 ; 10( 8): 593-599.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/(sici)1099-1395(199708)10:8%3C593::aid-poc926%3E3.0.co;2-h
    • Vancouver

      Stevani CV, Baader WJ. Kinetic studies on the chemiluminescent decomposition of an isolated intermediatin the peroxyoxylate reaction [Internet]. Journal of Physical Organic Chemistry. 1997 ; 10( 8): 593-599.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/(sici)1099-1395(199708)10:8%3C593::aid-poc926%3E3.0.co;2-h
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      EL SEOUD, Omar A e MARTINS, Monica F. Kinetics and mechanism of the hydrolysis of substituted phenylbenzoates catalyzed by the o-iodosobenzoate anion. Journal of Physical Organic Chemistry, v. 8 , n. 10, p. 637-46, 1995Tradução . . Disponível em: https://doi.org/10.1002/poc.610081003. Acesso em: 11 dez. 2025.
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      El Seoud, O. A., & Martins, M. F. (1995). Kinetics and mechanism of the hydrolysis of substituted phenylbenzoates catalyzed by the o-iodosobenzoate anion. Journal of Physical Organic Chemistry, 8 ( 10), 637-46. doi:10.1002/poc.610081003
    • NLM

      El Seoud OA, Martins MF. Kinetics and mechanism of the hydrolysis of substituted phenylbenzoates catalyzed by the o-iodosobenzoate anion [Internet]. Journal of Physical Organic Chemistry. 1995 ;8 ( 10): 637-46.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.610081003
    • Vancouver

      El Seoud OA, Martins MF. Kinetics and mechanism of the hydrolysis of substituted phenylbenzoates catalyzed by the o-iodosobenzoate anion [Internet]. Journal of Physical Organic Chemistry. 1995 ;8 ( 10): 637-46.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.610081003
  • Source: Journal of Physical Organic Chemistry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      EL SEOUD, Omar A et al. Kinetics and mechanism of the imidazole -catalysed hydrolysis of substituted n-benzoylimidazoles. Journal of Physical Organic Chemistry, v. 7 , n. 8 , p. 431-6, 1994Tradução . . Disponível em: https://doi.org/10.1002/poc.610070807. Acesso em: 11 dez. 2025.
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      El Seoud, O. A., Menegheli, P., Pires, P. A. R., & Kiyan, N. Z. (1994). Kinetics and mechanism of the imidazole -catalysed hydrolysis of substituted n-benzoylimidazoles. Journal of Physical Organic Chemistry, 7 ( 8 ), 431-6. doi:10.1002/poc.610070807
    • NLM

      El Seoud OA, Menegheli P, Pires PAR, Kiyan NZ. Kinetics and mechanism of the imidazole -catalysed hydrolysis of substituted n-benzoylimidazoles [Internet]. Journal of Physical Organic Chemistry. 1994 ;7 ( 8 ): 431-6.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.610070807
    • Vancouver

      El Seoud OA, Menegheli P, Pires PAR, Kiyan NZ. Kinetics and mechanism of the imidazole -catalysed hydrolysis of substituted n-benzoylimidazoles [Internet]. Journal of Physical Organic Chemistry. 1994 ;7 ( 8 ): 431-6.[citado 2025 dez. 11 ] Available from: https://doi.org/10.1002/poc.610070807

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