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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
Fonte: Synlett. Unidade: FFCLRP
Assuntos: 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: 29 set. 2024.
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 2024 set. 29 ] 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 2024 set. 29 ] 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
Fonte: Beilstein Journal of Organic Chemistry. Unidade: FFCLRP
Assuntos: 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: 29 set. 2024.
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 2024 set. 29 ] 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 2024 set. 29 ] 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
Fonte: Synthesis. Unidade: FFCLRP
Assuntos: 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: 29 set. 2024.
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 2024 set. 29 ] 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 2024 set. 29 ] Available from: https://doi.org/10.1055/s-0037-1610727
Artigo de periodico
Green synthesis from biomass (2014)
Donate, Paulo Marcos
Fonte: Chemical and Biological Technologies in Agriculture. Unidade: FFCLRP
Assuntos: 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: 29 set. 2024.
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 2024 set. 29 ] 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 2024 set. 29 ] 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.
Fonte: Planta Medica. Nome do evento: Annual Oxford International Conference on the Science of Botanicals. Unidades: FCFRP, FFCLRP
Assunto: TRYPANOSOMA
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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: 29 set. 2024. , 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 2024 set. 29 ]
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 2024 set. 29 ]
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
Fonte: 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: 29 set. 2024.
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 2024 set. 29 ] 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 2024 set. 29 ] Available from: https://doi.org/10.1007/s00436-006-0327-4

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