Filtros : "IQ" "REAÇÕES QUÍMICAS" "Brasil" Removidos: "Camargo, Pedro Henrique Cury de" "ROCCA, ROSANA AMICI DELLA" Limpar

Filtros



Refine with date range


  • Source: Biosensors. Unidade: IQ

    Subjects: LUMINESCÊNCIA, REAÇÕES QUÍMICAS, BIOLUMINESCÊNCIA

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

      CABELLO, Maidileyvis Castro et al. The molecular basis of organic Chemiluminescence. Biosensors, v. 13, p. 1-21 art. 452, 2023Tradução . . Disponível em: https://doi.org/10.3390/bios13040452. Acesso em: 02 jul. 2024.
    • APA

      Cabello, M. C., Bartoloni, F. H., Bastos, E. L., & Baader, W. J. (2023). The molecular basis of organic Chemiluminescence. Biosensors, 13, 1-21 art. 452. doi:10.3390/bios13040452
    • NLM

      Cabello MC, Bartoloni FH, Bastos EL, Baader WJ. The molecular basis of organic Chemiluminescence [Internet]. Biosensors. 2023 ; 13 1-21 art. 452.[citado 2024 jul. 02 ] Available from: https://doi.org/10.3390/bios13040452
    • Vancouver

      Cabello MC, Bartoloni FH, Bastos EL, Baader WJ. The molecular basis of organic Chemiluminescence [Internet]. Biosensors. 2023 ; 13 1-21 art. 452.[citado 2024 jul. 02 ] Available from: https://doi.org/10.3390/bios13040452
  • Source: Abstracts. Conference titles: International Conference On e-Science (e-Science). Unidades: IQ, BIOINFORMÁTICA

    Subjects: CINÉTICA, REAÇÕES QUÍMICAS

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

      MONTONI, Fabio et al. Anguix: cell signaling modeling improvement through Sabio-RK association to reactome. 2022, Anais.. Salt Lake City: IEEE, 2022. Disponível em: https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=9973605. Acesso em: 02 jul. 2024.
    • APA

      Montoni, F., Sousa, R. N. de, Lima Junior, M. B. de, Campos, C. G. S., Wang, W., Constantino, V. M., et al. (2022). Anguix: cell signaling modeling improvement through Sabio-RK association to reactome. In Abstracts. Salt Lake City: IEEE. Recuperado de https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=9973605
    • NLM

      Montoni F, Sousa RN de, Lima Junior MB de, Campos CGS, Wang W, Constantino VM, Santos CS, Armelin HA, Reis MS. Anguix: cell signaling modeling improvement through Sabio-RK association to reactome [Internet]. Abstracts. 2022 ;[citado 2024 jul. 02 ] Available from: https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=9973605
    • Vancouver

      Montoni F, Sousa RN de, Lima Junior MB de, Campos CGS, Wang W, Constantino VM, Santos CS, Armelin HA, Reis MS. Anguix: cell signaling modeling improvement through Sabio-RK association to reactome [Internet]. Abstracts. 2022 ;[citado 2024 jul. 02 ] Available from: https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=9973605
  • Source: Problems of Education in the 21st Century. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, ENSINO E APRENDIZAGEM

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

      GOES, Luciane F e NOGUEIRA, keysy S. C e FERNANDEZ, Carmen. Limitations of teaching and learning redox: a systematic review. Problems of Education in the 21st Century, v. 78, n. 5, p. 698-718, 2020Tradução . . Disponível em: https://doi.org/10.33225/pec/20.78.698. Acesso em: 02 jul. 2024.
    • APA

      Goes, L. F., Nogueira, keysy S. C., & Fernandez, C. (2020). Limitations of teaching and learning redox: a systematic review. Problems of Education in the 21st Century, 78( 5), 698-718. doi:10.33225/pec/20.78.698
    • NLM

      Goes LF, Nogueira keysy SC, Fernandez C. Limitations of teaching and learning redox: a systematic review [Internet]. Problems of Education in the 21st Century. 2020 ; 78( 5): 698-718.[citado 2024 jul. 02 ] Available from: https://doi.org/10.33225/pec/20.78.698
    • Vancouver

      Goes LF, Nogueira keysy SC, Fernandez C. Limitations of teaching and learning redox: a systematic review [Internet]. Problems of Education in the 21st Century. 2020 ; 78( 5): 698-718.[citado 2024 jul. 02 ] Available from: https://doi.org/10.33225/pec/20.78.698
  • Source: Advanced Synthesis and Catalysis. Unidade: IQ

    Subjects: CATÁLISE ASSIMÉTRICA, REAÇÕES QUÍMICAS, PALÁDIO

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

      POLO, Ellen Christine et al. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, v. 362, p. 884 – 892, 2020Tradução . . Disponível em: https://doi.org/10.1002/adsc.201901471. Acesso em: 02 jul. 2024.
    • APA

      Polo, E. C., Wang, M. F., Angnes, R. A., Braga, A. A. C., & Correia, C. R. D. (2020). Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity. Advanced Synthesis and Catalysis, 362, 884 – 892. doi:10.1002/adsc.201901471
    • NLM

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1002/adsc.201901471
    • Vancouver

      Polo EC, Wang MF, Angnes RA, Braga AAC, Correia CRD. Enantioselective heck arylation of acyclic alkenol aryl ethers: synthetic applications and DFT investigation of the stereoselectivity [Internet]. Advanced Synthesis and Catalysis. 2020 ; 362 884 – 892.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1002/adsc.201901471
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, SÍNTESE ORGÂNICA

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

      SILVA, Vitor Hugo Menezes da et al. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, v. 896, p. 5-15, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2019.05.023. Acesso em: 02 jul. 2024.
    • APA

      Silva, V. H. M. da, Morgon, N. H., Correia, C. R. D., & Braga, A. A. C. (2019). DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts. Journal of Organometallic Chemistry, 896, 5-15. doi:10.1016/j.jorganchem.2019.05.023
    • NLM

      Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023
    • Vancouver

      Silva VHM da, Morgon NH, Correia CRD, Braga AAC. DFT perspective on the selectivity and mechanism of ligand-free Heck reaction involving allylic esters and arenediazonium salts [Internet]. Journal of Organometallic Chemistry. 2019 ; 896 5-15.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1016/j.jorganchem.2019.05.023
  • Source: Photochemistry and Photobiology. Unidade: IQ

    Subjects: OXIDAÇÃO, REAÇÕES QUÍMICAS

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

      BAPTISTA, Maurício da Silva et al. Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways. Photochemistry and Photobiology, v. 93, p. 912-919, 2017Tradução . . Disponível em: https://doi.org/10.1111/php.12716. Acesso em: 02 jul. 2024.
    • APA

      Baptista, M. da S., Cadet, J., Di Mascio, P., Ghogare, A. A., Greer, A., Hamblin, M., et al. (2017). Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways. Photochemistry and Photobiology, 93, 912-919. doi:10.1111/php.12716
    • NLM

      Baptista M da S, Cadet J, Di Mascio P, Ghogare AA, Greer A, Hamblin M, Lorente C, Núñez SC, Ribeiro MS, Thomas AH, Vignoni M, Yoshimura TM. Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways [Internet]. Photochemistry and Photobiology. 2017 ; 93 912-919.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1111/php.12716
    • Vancouver

      Baptista M da S, Cadet J, Di Mascio P, Ghogare AA, Greer A, Hamblin M, Lorente C, Núñez SC, Ribeiro MS, Thomas AH, Vignoni M, Yoshimura TM. Type I and type II photosensitized oxidation reactions: guidelines and mechanistic pathways [Internet]. Photochemistry and Photobiology. 2017 ; 93 912-919.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1111/php.12716
  • Source: ChemistryOpen. Unidade: IQ

    Subjects: FÍSICO-QUÍMICA, REAÇÕES QUÍMICAS

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

      LEITAO, Ezequiel F. V et al. Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction. ChemistryOpen, v. 6, p. 360 –363, 2017Tradução . . Disponível em: https://doi.org/10.1002/open.201600169. Acesso em: 02 jul. 2024.
    • APA

      Leitao, E. F. V., Ventura, E., Souza, M. A. F. de, Riveros, J. M., & Monte, S. A. (2017). Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction. ChemistryOpen, 6, 360 –363. doi:10.1002/open.201600169
    • NLM

      Leitao EFV, Ventura E, Souza MAF de, Riveros JM, Monte SA. Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction [Internet]. ChemistryOpen. 2017 ; 6 360 –363.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1002/open.201600169
    • Vancouver

      Leitao EFV, Ventura E, Souza MAF de, Riveros JM, Monte SA. Spin-forbidden branching in the mechanism of the intrinsic haber-weiss reaction [Internet]. ChemistryOpen. 2017 ; 6 360 –363.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1002/open.201600169
  • Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: IQ

    Subjects: REAÇÕES QUÍMICAS, FORMAÇÃO DE PROFESSORES, QUÍMICA

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

      ALBUQUERQUE, Gabriela Zuleide Correia et al. Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 02 jul. 2024.
    • APA

      Albuquerque, G. Z. C., Vairolette, L. E., Rocha, F., Goes, L. F. de, Fernandez, C., & Agostinho, S. M. L. (2017). Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
    • NLM

      Albuquerque GZC, Vairolette LE, Rocha F, Goes LF de, Fernandez C, Agostinho SML. Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium [Internet]. Proceedings. 2017 ;[citado 2024 jul. 02 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
    • Vancouver

      Albuquerque GZC, Vairolette LE, Rocha F, Goes LF de, Fernandez C, Agostinho SML. Difficulties of chemistry teachers in the representation of chemical transformations in aqueous medium [Internet]. Proceedings. 2017 ;[citado 2024 jul. 02 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
  • Source: Journal of Computational Chemistry. Unidade: IQ

    Subjects: SINCRONICIDADE, REAÇÕES QUÍMICAS

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

      SOUZA, Miguel A. F. de et al. Revisiting the concept of the (a)synchronicityof diels-alder reactions based on the dynamicsof quasiclassical trajectories. Journal of Computational Chemistry, v. 37, n. 8, p. 701-711, 2016Tradução . . Disponível em: https://doi.org/10.1002/jcc.24245. Acesso em: 02 jul. 2024.
    • APA

      Souza, M. A. F. de, Ventura, E., Monte, S. A. do, Riveros, J. M., & Longo, R. L. (2016). Revisiting the concept of the (a)synchronicityof diels-alder reactions based on the dynamicsof quasiclassical trajectories. Journal of Computational Chemistry, 37( 8), 701-711. doi:10.1002/jcc.24245
    • NLM

      Souza MAF de, Ventura E, Monte SA do, Riveros JM, Longo RL. Revisiting the concept of the (a)synchronicityof diels-alder reactions based on the dynamicsof quasiclassical trajectories [Internet]. Journal of Computational Chemistry. 2016 ; 37( 8): 701-711.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1002/jcc.24245
    • Vancouver

      Souza MAF de, Ventura E, Monte SA do, Riveros JM, Longo RL. Revisiting the concept of the (a)synchronicityof diels-alder reactions based on the dynamicsof quasiclassical trajectories [Internet]. Journal of Computational Chemistry. 2016 ; 37( 8): 701-711.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1002/jcc.24245
  • Source: Journal of Organic Chemistry. Unidade: IQ

    Subjects: SOLVENTE, CATÁLISE, REAÇÕES QUÍMICAS

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

      SILVA, Juliana de Oliveira et al. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, v. 81, n. 5, p. 2010-2018, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.5b02846. Acesso em: 02 jul. 2024.
    • APA

      Silva, J. de O., Angnes, R. A., Silva, V. H. M. da, Servilha, B. M., Adeel, M., Braga, A. A. C., et al. (2016). Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds. Journal of Organic Chemistry, 81( 5), 2010-2018. doi:10.1021/acs.joc.5b02846
    • NLM

      Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1021/acs.joc.5b02846
    • Vancouver

      Silva J de O, Angnes RA, Silva VHM da, Servilha BM, Adeel M, Braga AAC, Aponick A, Correia CRD. Intermolecular noncovalent hydroxy directed enantioselective heck desymmetrization of cyclopentenol: computationally driven synthesis of highly functionalized cis-4-Arylcyclopentenol Scaffolds [Internet]. Journal of Organic Chemistry. 2016 ; 81( 5): 2010-2018.[citado 2024 jul. 02 ] Available from: https://doi.org/10.1021/acs.joc.5b02846

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024