Filtros : "REAÇÕES QUÍMICAS" "Indexado no Medline" Removido: "1987" Limpar

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  • Source: Journal of Colloid and Interface Science. Unidade: FFCLRP

    Subjects: REAÇÕES QUÍMICAS, TERMOGRAVIMETRIA

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    • ABNT

      DE OLIVEIRA, Edimar et al. Hexagonal mesoporous silica modified with copper phthalocyanine as a photocatalyst for pesticide 2,4-dichlorophenoxiacetic acid degradation. Journal of Colloid and Interface Science, v. 323, n. 1, p. 98-104, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jcis.2008.04.025. Acesso em: 17 out. 2024.
    • APA

      De Oliveira, E., Neri, C. R., Ribeiro, A. O., Garcia, V. S., Costa, L. L., Moura, A. O., et al. (2008). Hexagonal mesoporous silica modified with copper phthalocyanine as a photocatalyst for pesticide 2,4-dichlorophenoxiacetic acid degradation. Journal of Colloid and Interface Science, 323( 1), 98-104. doi:10.1016/j.jcis.2008.04.025
    • NLM

      De Oliveira E, Neri CR, Ribeiro AO, Garcia VS, Costa LL, Moura AO, Prado AGS, Serra OA, Iamamoto Y. Hexagonal mesoporous silica modified with copper phthalocyanine as a photocatalyst for pesticide 2,4-dichlorophenoxiacetic acid degradation [Internet]. Journal of Colloid and Interface Science. 2008 ; 323( 1): 98-104.[citado 2024 out. 17 ] Available from: https://doi.org/10.1016/j.jcis.2008.04.025
    • Vancouver

      De Oliveira E, Neri CR, Ribeiro AO, Garcia VS, Costa LL, Moura AO, Prado AGS, Serra OA, Iamamoto Y. Hexagonal mesoporous silica modified with copper phthalocyanine as a photocatalyst for pesticide 2,4-dichlorophenoxiacetic acid degradation [Internet]. Journal of Colloid and Interface Science. 2008 ; 323( 1): 98-104.[citado 2024 out. 17 ] Available from: https://doi.org/10.1016/j.jcis.2008.04.025
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: REAÇÕES QUÍMICAS

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      GUERRERO JÚNIOR, Palimécio G. e DABDOUB, Miguel Joaquim e BARONI, Adriano C. M. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals. Tetrahedron Letters, v. 49, n. 24, p. 3872-3876, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.04.072. Acesso em: 17 out. 2024.
    • APA

      Guerrero Júnior, P. G., Dabdoub, M. J., & Baroni, A. C. M. (2008). Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals. Tetrahedron Letters, 49( 24), 3872-3876. doi:10.1016/j.tetlet.2008.04.072
    • NLM

      Guerrero Júnior PG, Dabdoub MJ, Baroni ACM. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3872-3876.[citado 2024 out. 17 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.072
    • Vancouver

      Guerrero Júnior PG, Dabdoub MJ, Baroni ACM. Hydroalumination of selenoacetylenes: a versatile generation and reaction of 'alfa'-aluminate vinyl selenide intermediates in the highly regio and stereoselective synthesis of telluro(seleno)ketene acetals [Internet]. Tetrahedron Letters. 2008 ; 49( 24): 3872-3876.[citado 2024 out. 17 ] Available from: https://doi.org/10.1016/j.tetlet.2008.04.072
  • Source: Chemical Research in Toxicology. Unidade: IQ

    Subjects: BIOQUÍMICA, REAÇÕES QUÍMICAS

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      ROYER, Leandro de Oliveira et al. Peroxynitrite-initiated oxidation of acetoacetate and 2-methylacetoacetate esters by oxygen: potential sources of reactive intermediates in keto acidoses. Chemical Research in Toxicology, v. 17, n. 12, p. 1725-1732, 2004Tradução . . Acesso em: 17 out. 2024.
    • APA

      Royer, L. de O., Knudsen, F. da S., Oliveira, M. A. L. de, Tavares, M. F. M., & Bechara, E. J. H. (2004). Peroxynitrite-initiated oxidation of acetoacetate and 2-methylacetoacetate esters by oxygen: potential sources of reactive intermediates in keto acidoses. Chemical Research in Toxicology, 17( 12), 1725-1732.
    • NLM

      Royer L de O, Knudsen F da S, Oliveira MAL de, Tavares MFM, Bechara EJH. Peroxynitrite-initiated oxidation of acetoacetate and 2-methylacetoacetate esters by oxygen: potential sources of reactive intermediates in keto acidoses. Chemical Research in Toxicology. 2004 ; 17( 12): 1725-1732.[citado 2024 out. 17 ]
    • Vancouver

      Royer L de O, Knudsen F da S, Oliveira MAL de, Tavares MFM, Bechara EJH. Peroxynitrite-initiated oxidation of acetoacetate and 2-methylacetoacetate esters by oxygen: potential sources of reactive intermediates in keto acidoses. Chemical Research in Toxicology. 2004 ; 17( 12): 1725-1732.[citado 2024 out. 17 ]
  • Source: Chemical Research in Toxicology. Unidade: IQ

    Subjects: BIOQUÍMICA, REAÇÕES QUÍMICAS

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    • ABNT

      ROYER, Leandro de Oliveira et al. Succinylacetone oxidation by oxygen/peroxynitrite: a possible source of reactive intermediates in hereditary tyrosinemia type I. Chemical Research in Toxicology, v. 17, n. 5, p. 598-604, 2004Tradução . . Acesso em: 17 out. 2024.
    • APA

      Royer, L. de O., Knudsen, F. da S., Oliveira, M. A. L. de, Tavares, M. F. M., & Bechara, E. J. H. (2004). Succinylacetone oxidation by oxygen/peroxynitrite: a possible source of reactive intermediates in hereditary tyrosinemia type I. Chemical Research in Toxicology, 17( 5), 598-604.
    • NLM

      Royer L de O, Knudsen F da S, Oliveira MAL de, Tavares MFM, Bechara EJH. Succinylacetone oxidation by oxygen/peroxynitrite: a possible source of reactive intermediates in hereditary tyrosinemia type I. Chemical Research in Toxicology. 2004 ; 17( 5): 598-604.[citado 2024 out. 17 ]
    • Vancouver

      Royer L de O, Knudsen F da S, Oliveira MAL de, Tavares MFM, Bechara EJH. Succinylacetone oxidation by oxygen/peroxynitrite: a possible source of reactive intermediates in hereditary tyrosinemia type I. Chemical Research in Toxicology. 2004 ; 17( 5): 598-604.[citado 2024 out. 17 ]
  • Source: Biochemical and Biophysical Research Communications. Unidade: IQ

    Subjects: CATÁLISE, REAÇÕES QUÍMICAS

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    • ABNT

      MARANA, Sandro Roberto et al. Subsites of trypsin active site favor catalysis or substrate binding. Biochemical and Biophysical Research Communications, v. 290, n. 1, p. 494-497, 2002Tradução . . Disponível em: https://doi.org/10.1006/bbrc.2001.6172. Acesso em: 17 out. 2024.
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      Marana, S. R., Lopes, A. R., Juliano, L., Juliano, M. A., Ferreira, C., & Terra, W. R. (2002). Subsites of trypsin active site favor catalysis or substrate binding. Biochemical and Biophysical Research Communications, 290( 1), 494-497. doi:10.1006/bbrc.2001.6172
    • NLM

      Marana SR, Lopes AR, Juliano L, Juliano MA, Ferreira C, Terra WR. Subsites of trypsin active site favor catalysis or substrate binding [Internet]. Biochemical and Biophysical Research Communications. 2002 ; 290( 1): 494-497.[citado 2024 out. 17 ] Available from: https://doi.org/10.1006/bbrc.2001.6172
    • Vancouver

      Marana SR, Lopes AR, Juliano L, Juliano MA, Ferreira C, Terra WR. Subsites of trypsin active site favor catalysis or substrate binding [Internet]. Biochemical and Biophysical Research Communications. 2002 ; 290( 1): 494-497.[citado 2024 out. 17 ] Available from: https://doi.org/10.1006/bbrc.2001.6172
  • Source: Chemistry - A European Journal. Unidade: IQ

    Subjects: FÍSICO-QUÍMICA, HIDRÓLISE, REAÇÕES QUÍMICAS

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      PLIEGO JÚNIOR, Josefredo R. e RIVEROS, José Manuel. A theoretical analysis of the free-energy profile of the different pathways in the alkaline hydrolysis of methyl formate in aqueous solution. Chemistry - A European Journal, v. 8, n. 8, p. 1945-1953, 2002Tradução . . Acesso em: 17 out. 2024.
    • APA

      Pliego Júnior, J. R., & Riveros, J. M. (2002). A theoretical analysis of the free-energy profile of the different pathways in the alkaline hydrolysis of methyl formate in aqueous solution. Chemistry - A European Journal, 8( 8), 1945-1953.
    • NLM

      Pliego Júnior JR, Riveros JM. A theoretical analysis of the free-energy profile of the different pathways in the alkaline hydrolysis of methyl formate in aqueous solution. Chemistry - A European Journal. 2002 ; 8( 8): 1945-1953.[citado 2024 out. 17 ]
    • Vancouver

      Pliego Júnior JR, Riveros JM. A theoretical analysis of the free-energy profile of the different pathways in the alkaline hydrolysis of methyl formate in aqueous solution. Chemistry - A European Journal. 2002 ; 8( 8): 1945-1953.[citado 2024 out. 17 ]

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