Filtros : "Insuasty, Braulio" Limpar

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  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: ELÉTRONS, CORANTES, FOTOQUÍMICA

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    • ABNT

      REINA, Mauricio Caicedo et al. New organic photosensitizers based on triphenylamine and hydantoin as anchoring group onto TiO2 Surface. Journal of Molecular Structure, v. 1251, p. 1-8, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2021.132072. Acesso em: 28 maio 2024.
    • APA

      Reina, M. C., Guimarães, R. R., Ortiz, A., Araki, K., & Insuasty, B. (2021). New organic photosensitizers based on triphenylamine and hydantoin as anchoring group onto TiO2 Surface. Journal of Molecular Structure, 1251, 1-8. doi:10.1016/j.molstruc.2021.132072
    • NLM

      Reina MC, Guimarães RR, Ortiz A, Araki K, Insuasty B. New organic photosensitizers based on triphenylamine and hydantoin as anchoring group onto TiO2 Surface [Internet]. Journal of Molecular Structure. 2021 ; 1251 1-8.[citado 2024 maio 28 ] Available from: https://doi.org/10.1016/j.molstruc.2021.132072
    • Vancouver

      Reina MC, Guimarães RR, Ortiz A, Araki K, Insuasty B. New organic photosensitizers based on triphenylamine and hydantoin as anchoring group onto TiO2 Surface [Internet]. Journal of Molecular Structure. 2021 ; 1251 1-8.[citado 2024 maio 28 ] Available from: https://doi.org/10.1016/j.molstruc.2021.132072
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: COMPOSTOS HETEROCÍCLICOS, ELETROQUÍMICA

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    • ABNT

      CAICEDO, Mauricio et al. Microwave assisted synthesis of a series of charge-transfer photosensitizers having quinoxaline-2(1H)-one as anchoring group onto TiO2 surface. Journal of Molecular Structure, v. 1133, p. 384-391, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2016.12.021. Acesso em: 28 maio 2024.
    • APA

      Caicedo, M., Echeverry, C. A., Guimarães, R. R., Ortiz, A., Araki, K., & Insuasty, B. (2017). Microwave assisted synthesis of a series of charge-transfer photosensitizers having quinoxaline-2(1H)-one as anchoring group onto TiO2 surface. Journal of Molecular Structure, 1133, 384-391. doi:10.1016/j.molstruc.2016.12.021
    • NLM

      Caicedo M, Echeverry CA, Guimarães RR, Ortiz A, Araki K, Insuasty B. Microwave assisted synthesis of a series of charge-transfer photosensitizers having quinoxaline-2(1H)-one as anchoring group onto TiO2 surface [Internet]. Journal of Molecular Structure. 2017 ; 1133 384-391.[citado 2024 maio 28 ] Available from: https://doi.org/10.1016/j.molstruc.2016.12.021
    • Vancouver

      Caicedo M, Echeverry CA, Guimarães RR, Ortiz A, Araki K, Insuasty B. Microwave assisted synthesis of a series of charge-transfer photosensitizers having quinoxaline-2(1H)-one as anchoring group onto TiO2 surface [Internet]. Journal of Molecular Structure. 2017 ; 1133 384-391.[citado 2024 maio 28 ] Available from: https://doi.org/10.1016/j.molstruc.2016.12.021
  • Source: Journal of Molecular Structure. Unidade: IQ

    Subjects: CORANTES, FOTOQUÍMICA, ELETROQUÍMICA

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    • ABNT

      ARCOS, Wilmmer A et al. Structural effects on the photoelectrochemical properties of new push-pull dyes based on vinazene acceptor triphenylamine donor. Journal of Molecular Structure, v. 1111, n. 5, p. 157-165, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2016.01.087. Acesso em: 28 maio 2024.
    • APA

      Arcos, W. A., Guimarães, R. R., Insuasty, B., Araki, K., & Ortiz, A. (2016). Structural effects on the photoelectrochemical properties of new push-pull dyes based on vinazene acceptor triphenylamine donor. Journal of Molecular Structure, 1111( 5), 157-165. doi:10.1016/j.molstruc.2016.01.087
    • NLM

      Arcos WA, Guimarães RR, Insuasty B, Araki K, Ortiz A. Structural effects on the photoelectrochemical properties of new push-pull dyes based on vinazene acceptor triphenylamine donor [Internet]. Journal of Molecular Structure. 2016 ; 1111( 5): 157-165.[citado 2024 maio 28 ] Available from: https://doi.org/10.1016/j.molstruc.2016.01.087
    • Vancouver

      Arcos WA, Guimarães RR, Insuasty B, Araki K, Ortiz A. Structural effects on the photoelectrochemical properties of new push-pull dyes based on vinazene acceptor triphenylamine donor [Internet]. Journal of Molecular Structure. 2016 ; 1111( 5): 157-165.[citado 2024 maio 28 ] Available from: https://doi.org/10.1016/j.molstruc.2016.01.087
  • Source: Journal of Heterocyclic Chemistry. Unidade: IQSC

    Assunto: QUÍMICA

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    • ABNT

      QUIROGA, Jairo et al. Synthesis of 5-Cyanopyrazolo[3,4-b]pyridines in the reaction of 5-Amino-3-methyl-1-phenylpyrazole with Arylidene derivatives of malonodinitrile and Ethyl Cyanoacetate. Journal of Heterocyclic Chemistry, v. 36, n. 5, p. 1311-1316, 1999Tradução . . Disponível em: https://doi.org/10.1002/jhet.5570360533. Acesso em: 28 maio 2024.
    • APA

      Quiroga, J., Alvarado, M., Insuasty, B., Moreno, R., Ravina, E., Estevez, I., & Santos, R. H. de A. (1999). Synthesis of 5-Cyanopyrazolo[3,4-b]pyridines in the reaction of 5-Amino-3-methyl-1-phenylpyrazole with Arylidene derivatives of malonodinitrile and Ethyl Cyanoacetate. Journal of Heterocyclic Chemistry, 36( 5), 1311-1316. doi:10.1002/jhet.5570360533
    • NLM

      Quiroga J, Alvarado M, Insuasty B, Moreno R, Ravina E, Estevez I, Santos RH de A. Synthesis of 5-Cyanopyrazolo[3,4-b]pyridines in the reaction of 5-Amino-3-methyl-1-phenylpyrazole with Arylidene derivatives of malonodinitrile and Ethyl Cyanoacetate [Internet]. Journal of Heterocyclic Chemistry. 1999 ; 36( 5): 1311-1316.[citado 2024 maio 28 ] Available from: https://doi.org/10.1002/jhet.5570360533
    • Vancouver

      Quiroga J, Alvarado M, Insuasty B, Moreno R, Ravina E, Estevez I, Santos RH de A. Synthesis of 5-Cyanopyrazolo[3,4-b]pyridines in the reaction of 5-Amino-3-methyl-1-phenylpyrazole with Arylidene derivatives of malonodinitrile and Ethyl Cyanoacetate [Internet]. Journal of Heterocyclic Chemistry. 1999 ; 36( 5): 1311-1316.[citado 2024 maio 28 ] Available from: https://doi.org/10.1002/jhet.5570360533
  • Source: Journal of Heterocyclic Chemistry. Unidade: IQSC

    Assunto: QUÍMICA

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    • ABNT

      INSUASTY, Braulio et al. Synthesis of 2-(p-R-Benzoylmethylene)-3-(p-R-phenyl)-1H-quinoxalines. Journal of Heterocyclic Chemistry, v. 35, p. 977-981, 1998Tradução . . Disponível em: https://doi.org/10.1002/jhet.5570350432. Acesso em: 28 maio 2024.
    • APA

      Insuasty, B., Fernández, F., Quiroga, J., Moreno, R., Martínez, R., Angeles, E., et al. (1998). Synthesis of 2-(p-R-Benzoylmethylene)-3-(p-R-phenyl)-1H-quinoxalines. Journal of Heterocyclic Chemistry, 35, 977-981. doi:10.1002/jhet.5570350432
    • NLM

      Insuasty B, Fernández F, Quiroga J, Moreno R, Martínez R, Angeles E, Gaviño R, Santos RH de A. Synthesis of 2-(p-R-Benzoylmethylene)-3-(p-R-phenyl)-1H-quinoxalines [Internet]. Journal of Heterocyclic Chemistry. 1998 ; 35 977-981.[citado 2024 maio 28 ] Available from: https://doi.org/10.1002/jhet.5570350432
    • Vancouver

      Insuasty B, Fernández F, Quiroga J, Moreno R, Martínez R, Angeles E, Gaviño R, Santos RH de A. Synthesis of 2-(p-R-Benzoylmethylene)-3-(p-R-phenyl)-1H-quinoxalines [Internet]. Journal of Heterocyclic Chemistry. 1998 ; 35 977-981.[citado 2024 maio 28 ] Available from: https://doi.org/10.1002/jhet.5570350432
  • Source: Journal of Heterocyclic Chemistry. Unidade: IQSC

    Assunto: QUÍMICA

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    • ABNT

      QUIROGA, Jairo et al. Reaction of 5-aminopyrazoles with 'Beta'-Dimethylaminopropiophenones: Synthesis of new pyrazolo[3,4-b]pyridines. Journal of Heterocyclic Chemistry, v. 35, p. 333-338, 1998Tradução . . Acesso em: 28 maio 2024.
    • APA

      Quiroga, J., Insuasty, B., Cruz, S., Hernandez, P., Bolaños, A., Moreno, R., et al. (1998). Reaction of 5-aminopyrazoles with 'Beta'-Dimethylaminopropiophenones: Synthesis of new pyrazolo[3,4-b]pyridines. Journal of Heterocyclic Chemistry, 35, 333-338.
    • NLM

      Quiroga J, Insuasty B, Cruz S, Hernandez P, Bolaños A, Moreno R, Hormaza A, Santos RH de A. Reaction of 5-aminopyrazoles with 'Beta'-Dimethylaminopropiophenones: Synthesis of new pyrazolo[3,4-b]pyridines. Journal of Heterocyclic Chemistry. 1998 ; 35 333-338.[citado 2024 maio 28 ]
    • Vancouver

      Quiroga J, Insuasty B, Cruz S, Hernandez P, Bolaños A, Moreno R, Hormaza A, Santos RH de A. Reaction of 5-aminopyrazoles with 'Beta'-Dimethylaminopropiophenones: Synthesis of new pyrazolo[3,4-b]pyridines. Journal of Heterocyclic Chemistry. 1998 ; 35 333-338.[citado 2024 maio 28 ]
  • Source: European Journal of Organic Chemistry. Unidade: IQSC

    Assunto: QUÍMICA

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    • ABNT

      QUIROGA, Jairo et al. Generation of 6,7-Dihydro-5H-1,3,4-thiadiazolo[3,2-a]pyridines: unexpected products in the reaction of 5-Ethylthio-1,3-4-thiadiazole-2-amine and 3-(Dimethylamino)propiophenones. European Journal of Organic Chemistry, n. 6, p. 1201-1203, 1998Tradução . . Disponível em: https://doi.org/10.1002/(sici)1099-0690(199806)1998:6%3C1201::aid-ejoc1201%3E3.0.co;2-7. Acesso em: 28 maio 2024.
    • APA

      Quiroga, J., Insuasty, B., Hernandez, P., Moreno, R., Santos, R. H. de A., & Meier, H. (1998). Generation of 6,7-Dihydro-5H-1,3,4-thiadiazolo[3,2-a]pyridines: unexpected products in the reaction of 5-Ethylthio-1,3-4-thiadiazole-2-amine and 3-(Dimethylamino)propiophenones. European Journal of Organic Chemistry, (6), 1201-1203. doi:10.1002/(sici)1099-0690(199806)1998:6%3C1201::aid-ejoc1201%3E3.0.co;2-7
    • NLM

      Quiroga J, Insuasty B, Hernandez P, Moreno R, Santos RH de A, Meier H. Generation of 6,7-Dihydro-5H-1,3,4-thiadiazolo[3,2-a]pyridines: unexpected products in the reaction of 5-Ethylthio-1,3-4-thiadiazole-2-amine and 3-(Dimethylamino)propiophenones [Internet]. European Journal of Organic Chemistry. 1998 ;(6): 1201-1203.[citado 2024 maio 28 ] Available from: https://doi.org/10.1002/(sici)1099-0690(199806)1998:6%3C1201::aid-ejoc1201%3E3.0.co;2-7
    • Vancouver

      Quiroga J, Insuasty B, Hernandez P, Moreno R, Santos RH de A, Meier H. Generation of 6,7-Dihydro-5H-1,3,4-thiadiazolo[3,2-a]pyridines: unexpected products in the reaction of 5-Ethylthio-1,3-4-thiadiazole-2-amine and 3-(Dimethylamino)propiophenones [Internet]. European Journal of Organic Chemistry. 1998 ;(6): 1201-1203.[citado 2024 maio 28 ] Available from: https://doi.org/10.1002/(sici)1099-0690(199806)1998:6%3C1201::aid-ejoc1201%3E3.0.co;2-7

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