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  • Source: Advanced Synthesis & Catalysis. Unidade: FCFRP

    Subjects: SULFONAMIDAS, SÍNTESE QUÍMICA, FARMACOLOGIA

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    • ABNT

      ARROIO, Thais Rodrigues et al. Generation of sulfamoyl radicals via visible-light mediated fixation of sulfur dioxide for the synthesis of sulfonamides. Advanced Synthesis & Catalysis, v. 367, 2025Tradução . . Disponível em: https://doi.org/10.1002/adsc.202401065. Acesso em: 17 abr. 2026.
    • APA

      Arroio, T. R., Nau, J. P., Hofman, K., Förster, C., Faber, S. L., Becker, S., et al. (2025). Generation of sulfamoyl radicals via visible-light mediated fixation of sulfur dioxide for the synthesis of sulfonamides. Advanced Synthesis & Catalysis, 367. doi:10.1002/adsc.202401065
    • NLM

      Arroio TR, Nau JP, Hofman K, Förster C, Faber SL, Becker S, Heinze K, Clososki GC, Manolikakes G. Generation of sulfamoyl radicals via visible-light mediated fixation of sulfur dioxide for the synthesis of sulfonamides [Internet]. Advanced Synthesis & Catalysis. 2025 ; 367[citado 2026 abr. 17 ] Available from: https://doi.org/10.1002/adsc.202401065
    • Vancouver

      Arroio TR, Nau JP, Hofman K, Förster C, Faber SL, Becker S, Heinze K, Clososki GC, Manolikakes G. Generation of sulfamoyl radicals via visible-light mediated fixation of sulfur dioxide for the synthesis of sulfonamides [Internet]. Advanced Synthesis & Catalysis. 2025 ; 367[citado 2026 abr. 17 ] Available from: https://doi.org/10.1002/adsc.202401065
  • Source: Annals. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidade: IFSC

    Subjects: AGENTES ANTIMICROBIANOS, PLANEJAMENTO DE FÁRMACOS

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    • ABNT

      MOFATI, Átila Menegardo et al. Design, synthesis and evaluation of the antimalarial activity of chromenes obtained by Hantzsch multicomponent reactions. 2025, Anais.. Rio de Janeiro: Universidade Federal do Rio de Janeiro - UFRJ, 2025. Disponível em: https://repositorio.usp.br/directbitstream/a3e92c68-579a-4354-9869-9bce60e9d0b1/3290326.pdf. Acesso em: 17 abr. 2026.
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      Mofati, Á. M., Valdes, T. A., Guido, R. V. C., Graebin, C. S., & Kümmerle, A. E. (2025). Design, synthesis and evaluation of the antimalarial activity of chromenes obtained by Hantzsch multicomponent reactions. In Annals. Rio de Janeiro: Universidade Federal do Rio de Janeiro - UFRJ. Recuperado de https://repositorio.usp.br/directbitstream/a3e92c68-579a-4354-9869-9bce60e9d0b1/3290326.pdf
    • NLM

      Mofati ÁM, Valdes TA, Guido RVC, Graebin CS, Kümmerle AE. Design, synthesis and evaluation of the antimalarial activity of chromenes obtained by Hantzsch multicomponent reactions [Internet]. Annals. 2025 ;[citado 2026 abr. 17 ] Available from: https://repositorio.usp.br/directbitstream/a3e92c68-579a-4354-9869-9bce60e9d0b1/3290326.pdf
    • Vancouver

      Mofati ÁM, Valdes TA, Guido RVC, Graebin CS, Kümmerle AE. Design, synthesis and evaluation of the antimalarial activity of chromenes obtained by Hantzsch multicomponent reactions [Internet]. Annals. 2025 ;[citado 2026 abr. 17 ] Available from: https://repositorio.usp.br/directbitstream/a3e92c68-579a-4354-9869-9bce60e9d0b1/3290326.pdf
  • Source: Orbital: The Electronic Journal of Chemistry. Unidade: FFCLRP

    Subjects: RADIAÇÃO ELETROMAGNÉTICA, TECNOLOGIA DE MICRO-ONDAS, SOLVENTE

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    • ABNT

      DONATE, Paulo Marcos e BARBOSA, Hugo Elias. Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives. Orbital: The Electronic Journal of Chemistry, v. 13, n. 4, p. 376-384, 2021Tradução . . Disponível em: https://doi.org/10.17807/orbital.v13i4.1657. Acesso em: 17 abr. 2026.
    • APA

      Donate, P. M., & Barbosa, H. E. (2021). Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives. Orbital: The Electronic Journal of Chemistry, 13( 4), 376-384. doi:10.17807/orbital.v13i4.1657
    • NLM

      Donate PM, Barbosa HE. Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives [Internet]. Orbital: The Electronic Journal of Chemistry. 2021 ; 13( 4): 376-384.[citado 2026 abr. 17 ] Available from: https://doi.org/10.17807/orbital.v13i4.1657
    • Vancouver

      Donate PM, Barbosa HE. Microwave Radiation Applied to the Synthesis of ץ-butyrolactone Derivatives [Internet]. Orbital: The Electronic Journal of Chemistry. 2021 ; 13( 4): 376-384.[citado 2026 abr. 17 ] Available from: https://doi.org/10.17807/orbital.v13i4.1657
  • Source: Organics. Unidade: FCFRP

    Subjects: PRODUTOS NATURAIS, FÁRMACOS SINTÉTICOS

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    • ABNT

      WINANT, Pieterjan et al. A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones. Organics, v. 2, n. 2, p. 118-141, 2021Tradução . . Disponível em: https://doi.org/10.3390/org2020011. Acesso em: 17 abr. 2026.
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      Winant, P., Horsten, T., Melo, S. M. G. de, Emery, F. da S., & Dehaen, W. (2021). A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones. Organics, 2( 2), 118-141. doi:10.3390/org2020011
    • NLM

      Winant P, Horsten T, Melo SMG de, Emery F da S, Dehaen W. A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones [Internet]. Organics. 2021 ; 2( 2): 118-141.[citado 2026 abr. 17 ] Available from: https://doi.org/10.3390/org2020011
    • Vancouver

      Winant P, Horsten T, Melo SMG de, Emery F da S, Dehaen W. A review of the synthetic strategies toward Dihydropyrrolo [1,2-a] Pyrazinones [Internet]. Organics. 2021 ; 2( 2): 118-141.[citado 2026 abr. 17 ] Available from: https://doi.org/10.3390/org2020011
  • Source: Synthesis. Unidade: IFSC

    Subjects: QUÍMICA VERDE, PLANEJAMENTO DE FÁRMACOS

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    • ABNT

      SANTOS, Deborah A. et al. Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction. Synthesis, v. 52, n. 7, p. 1076-1086, 2020Tradução . . Disponível em: https://doi.org/10.1055/s-0039-1690774. Acesso em: 17 abr. 2026.
    • APA

      Santos, D. A., Silva, A. R., Ellena, J., Silva, C. C. P., Paixão, M. W., & Corrêa, A. G. (2020). Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction. Synthesis, 52( 7), 1076-1086. doi:10.1055/s-0039-1690774
    • NLM

      Santos DA, Silva AR, Ellena J, Silva CCP, Paixão MW, Corrêa AG. Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction [Internet]. Synthesis. 2020 ; 52( 7): 1076-1086.[citado 2026 abr. 17 ] Available from: https://doi.org/10.1055/s-0039-1690774
    • Vancouver

      Santos DA, Silva AR, Ellena J, Silva CCP, Paixão MW, Corrêa AG. Green one-pot asymmetric synthesis of peptidomimetics via sequential organocatalyzed aziridination and Passerini multicomponent reaction [Internet]. Synthesis. 2020 ; 52( 7): 1076-1086.[citado 2026 abr. 17 ] Available from: https://doi.org/10.1055/s-0039-1690774
  • Source: Journal of the Brazilian Chemical Society. Unidade: FFCLRP

    Subjects: QUÍMICA, PEPTÍDEOS, LEISHMANIA

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    • ABNT

      PREVIDI, Daniel et al. Synthesis and antileishmanial activity of some functionalized peptoids. Journal of the Brazilian Chemical Society, v. 30, n. 6, p. 1334-1340, 2019Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20190023. Acesso em: 17 abr. 2026.
    • APA

      Previdi, D., Rodrigues, S., Coelho, M. G., Candido, A. C. B. B., Magalhães, L. G., & Donate, P. M. (2019). Synthesis and antileishmanial activity of some functionalized peptoids. Journal of the Brazilian Chemical Society, 30( 6), 1334-1340. doi:10.21577/0103-5053.20190023
    • NLM

      Previdi D, Rodrigues S, Coelho MG, Candido ACBB, Magalhães LG, Donate PM. Synthesis and antileishmanial activity of some functionalized peptoids [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 6): 1334-1340.[citado 2026 abr. 17 ] Available from: https://doi.org/10.21577/0103-5053.20190023
    • Vancouver

      Previdi D, Rodrigues S, Coelho MG, Candido ACBB, Magalhães LG, Donate PM. Synthesis and antileishmanial activity of some functionalized peptoids [Internet]. Journal of the Brazilian Chemical Society. 2019 ; 30( 6): 1334-1340.[citado 2026 abr. 17 ] Available from: https://doi.org/10.21577/0103-5053.20190023

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