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Filtros : "DONATE, PAULO MARCOS" "Alemanha" Removido: "Abstract" Limpar

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  • Artigo de periodico

    Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes (2023)

    Baviera, Giovanni Stoppa; Donate, Paulo Marcos

    Source: Synlett. Unidade: FFCLRP

    Subjects: HIDROCARBONETOS POLICÍCLICOS, HIDROCARBONOS AROMÁTICOS, NIÓBIO, ÉTER

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    • ABNT

      BAVIERA, Giovanni Stoppa e DONATE, Paulo Marcos. Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes. Synlett, v. 34, n. 16, p. 1915-1919, 2023Tradução . . Disponível em: https://doi.org/10.1055/s-0041-1738445. Acesso em: 04 dez. 2025.

    • APA

      Baviera, G. S., & Donate, P. M. (2023). Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes. Synlett, 34( 16), 1915-1919. doi:10.1055/s-0041-1738445

    • NLM

      Baviera GS, Donate PM. Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes [Internet]. Synlett. 2023 ; 34( 16): 1915-1919.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1055/s-0041-1738445

    • Vancouver

      Baviera GS, Donate PM. Niobium pentachloride mediated direct bradsher-type reaction: a rapid and efficient strategy to synthesize novel substituted 9-anthraldehydes [Internet]. Synlett. 2023 ; 34( 16): 1915-1919.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1055/s-0041-1738445

  • Artigo de periodico

    Recent advances in the syntheses of anthracene derivatives (2021)

    Baviera, Giovanni Stoppa; Donate, Paulo Marcos

    Source: Beilstein Journal of Organic Chemistry. Unidade: FFCLRP

    Subjects: SÍNTESE QUÍMICA, POLÍMEROS (MATERIAIS), CÉLULAS SOLARES, HIDROCARBONETOS POLICÍCLICOS

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    • ABNT

      BAVIERA, Giovanni Stoppa e DONATE, Paulo Marcos. Recent advances in the syntheses of anthracene derivatives. Beilstein Journal of Organic Chemistry, v. 17, p. 2028-2050, 2021Tradução . . Disponível em: https://doi.org/10.3762/bjoc.17.131. Acesso em: 04 dez. 2025.

    • APA

      Baviera, G. S., & Donate, P. M. (2021). Recent advances in the syntheses of anthracene derivatives. Beilstein Journal of Organic Chemistry, 17, 2028-2050. doi:10.3762/bjoc.17.131

    • NLM

      Baviera GS, Donate PM. Recent advances in the syntheses of anthracene derivatives [Internet]. Beilstein Journal of Organic Chemistry. 2021 ; 17 2028-2050.[citado 2025 dez. 04 ] Available from: https://doi.org/10.3762/bjoc.17.131

    • Vancouver

      Baviera GS, Donate PM. Recent advances in the syntheses of anthracene derivatives [Internet]. Beilstein Journal of Organic Chemistry. 2021 ; 17 2028-2050.[citado 2025 dez. 04 ] Available from: https://doi.org/10.3762/bjoc.17.131

  • Artigo de periodico

    Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes (2019)

    Rodrigues, Shirley Muniz Machado; Previdi, Daniel; Baviera, Giovanni Stoppa; Matias, Alexandre A.; Donate, Paulo Marcos

    Source: Synthesis. Unidade: FFCLRP

    Subjects: COMPOSTOS ORGÂNICOS, NIÓBIO, ALDEÍDOS

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    • ABNT

      RODRIGUES, Shirley Muniz Machado et al. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes. Synthesis, v. 51, n. 23, p. 4498-4506, 2019Tradução . . Disponível em: https://doi.org/10.1055/s-0037-1610727. Acesso em: 04 dez. 2025.

    • APA

      Rodrigues, S. M. M., Previdi, D., Baviera, G. S., Matias, A. A., & Donate, P. M. (2019). Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes. Synthesis, 51( 23), 4498-4506. doi:10.1055/s-0037-1610727

    • NLM

      Rodrigues SMM, Previdi D, Baviera GS, Matias AA, Donate PM. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes [Internet]. Synthesis. 2019 ; 51( 23): 4498-4506.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1055/s-0037-1610727

    • Vancouver

      Rodrigues SMM, Previdi D, Baviera GS, Matias AA, Donate PM. Niobium pentachloride mediated (Hetero)aromatic aldehyde friedel–crafts hydroxyalkylation with arenes: an efficient strategy to synthesize triarylmethanes [Internet]. Synthesis. 2019 ; 51( 23): 4498-4506.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1055/s-0037-1610727

  • Artigo de periodico

    Green synthesis from biomass (2014)

    Donate, Paulo Marcos

    Source: Chemical and Biological Technologies in Agriculture. Unidade: FFCLRP

    Subjects: QUÍMICA VERDE, SÍNTESE QUÍMICA, BIOMASSA

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    • ABNT

      DONATE, Paulo Marcos. Green synthesis from biomass. Chemical and Biological Technologies in Agriculture, v. 1, 2014Tradução . . Disponível em: https://doi.org/10.1186/s40538-014-0004-2. Acesso em: 04 dez. 2025.

    • APA

      Donate, P. M. (2014). Green synthesis from biomass. Chemical and Biological Technologies in Agriculture, 1. doi:10.1186/s40538-014-0004-2

    • NLM

      Donate PM. Green synthesis from biomass [Internet]. Chemical and Biological Technologies in Agriculture. 2014 ; 1[citado 2025 dez. 04 ] Available from: https://doi.org/10.1186/s40538-014-0004-2

    • Vancouver

      Donate PM. Green synthesis from biomass [Internet]. Chemical and Biological Technologies in Agriculture. 2014 ; 1[citado 2025 dez. 04 ] Available from: https://doi.org/10.1186/s40538-014-0004-2

  • Trabalho de evento-resumo periodico

    Trypanocidal structure-activity relationship for Cis-and Trans-methylpluviatolide (2008)

    Silva, R.; Saraiva, J.; Albuquerque, Sérgio de; Curti, Carlos; Donate, Paulo Marcos; Bianco, T. N. C.; Bastos, Jairo Kenupp; Silva, M. L. A.

    Source: Planta Medica. Conference titles: Annual Oxford International Conference on the Science of Botanicals. Unidades: FCFRP, FFCLRP

    Assunto: TRYPANOSOMA

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    • ABNT

      SILVA, R. et al. Trypanocidal structure-activity relationship for Cis-and Trans-methylpluviatolide. Planta Medica. Stuttgart: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 04 dez. 2025. , 2008

    • APA

      Silva, R., Saraiva, J., Albuquerque, S. de, Curti, C., Donate, P. M., Bianco, T. N. C., et al. (2008). Trypanocidal structure-activity relationship for Cis-and Trans-methylpluviatolide. Planta Medica. Stuttgart: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo.

    • NLM

      Silva R, Saraiva J, Albuquerque S de, Curti C, Donate PM, Bianco TNC, Bastos JK, Silva MLA. Trypanocidal structure-activity relationship for Cis-and Trans-methylpluviatolide. Planta Medica. 2008 ; 74( 3):[citado 2025 dez. 04 ]

    • Vancouver

      Silva R, Saraiva J, Albuquerque S de, Curti C, Donate PM, Bianco TNC, Bastos JK, Silva MLA. Trypanocidal structure-activity relationship for Cis-and Trans-methylpluviatolide. Planta Medica. 2008 ; 74( 3):[citado 2025 dez. 04 ]

  • Artigo de periodico

    In vitro and in vivo activity of lignan lactones derivative against Trypanosoma cruzi (2007)

    Saraiva, Juliana; Vega, Celeste; Rolon, Mirian; Silva, Rosangela da; Silva, Márcio Luis Andrade e; Donate, Paulo Marcos; Bastos, Jairo Kenupp; Gomez-Barrio, Alícia; Albuquerque, Sérgio de

    Source: Parasitology Research. Unidades: FFCLRP, FCFRP

    Assunto: TRYPANOSOMA CRUZI (ESTUDO IN VITRO)

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    • ABNT

      SARAIVA, Juliana et al. In vitro and in vivo activity of lignan lactones derivative against Trypanosoma cruzi. Parasitology Research, v. 100, n. 4, p. 791-795, 2007Tradução . . Disponível em: https://doi.org/10.1007/s00436-006-0327-4. Acesso em: 04 dez. 2025.

    • APA

      Saraiva, J., Vega, C., Rolon, M., Silva, R. da, Silva, M. L. A. e, Donate, P. M., et al. (2007). In vitro and in vivo activity of lignan lactones derivative against Trypanosoma cruzi. Parasitology Research, 100( 4), 791-795. doi:10.1007/s00436-006-0327-4

    • NLM

      Saraiva J, Vega C, Rolon M, Silva R da, Silva MLA e, Donate PM, Bastos JK, Gomez-Barrio A, Albuquerque S de. In vitro and in vivo activity of lignan lactones derivative against Trypanosoma cruzi [Internet]. Parasitology Research. 2007 ; 100( 4): 791-795.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1007/s00436-006-0327-4

    • Vancouver

      Saraiva J, Vega C, Rolon M, Silva R da, Silva MLA e, Donate PM, Bastos JK, Gomez-Barrio A, Albuquerque S de. In vitro and in vivo activity of lignan lactones derivative against Trypanosoma cruzi [Internet]. Parasitology Research. 2007 ; 100( 4): 791-795.[citado 2025 dez. 04 ] Available from: https://doi.org/10.1007/s00436-006-0327-4
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