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Filtros : "COMPOSTOS ORGÂNICOS" "EMERY, FLAVIO DA SILVA" Removido: "Abstracts Book" Limpar

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1 - 8 (8 records)

  • Artigo de periodico

    Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties (2021)

    Mello, Rodrigo Brito de ; Emery, Flavio da Silva

    Source: Journal of Fluorescence. Unidade: FCFRP

    Subjects: CORANTES, QUÍMICA ORGÂNICA, COMPOSTOS ORGÂNICOS, SISTEMA QUÂNTICO

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    • ABNT

      MELLO, Rodrigo Brito de e EMERY, Flavio da Silva. Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties. Journal of Fluorescence, v. 32, n. 1, p. 81-86, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10895-021-02831-z. Acesso em: 27 nov. 2025.

    • APA

      Mello, R. B. de, & Emery, F. da S. (2021). Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties. Journal of Fluorescence, 32( 1), 81-86. doi:10.1007/s10895-021-02831-z

    • NLM

      Mello RB de, Emery F da S. Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties [Internet]. Journal of Fluorescence. 2021 ; 32( 1): 81-86.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1007/s10895-021-02831-z

    • Vancouver

      Mello RB de, Emery F da S. Impact of the arylation of fused N-bridged BODIPY dyes in photophysical properties [Internet]. Journal of Fluorescence. 2021 ; 32( 1): 81-86.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1007/s10895-021-02831-z

  • Artigo de periodico

    Nitrosation of BODIPY dyes and their applications in the development of thiol sensors (2020)

    Melo, Shaiani Maria Gil de; Rezende, Lucas Cunha Dias de; Petrilli, Raquel ; Lopez, Renata Fonseca Vianna ; Goulart, Marilia O. F.; Emery, Flavio da Silva

    Source: Dyes and Pigments. Unidade: FCFRP

    Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS, SENSORES QUÍMICOS, CORANTES FLUORESCENTES

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      MELO, Shaiani Maria Gil de et al. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors. Dyes and Pigments, v. 173, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.107885. Acesso em: 27 nov. 2025.

    • APA

      Melo, S. M. G. de, Rezende, L. C. D. de, Petrilli, R., Lopez, R. F. V., Goulart, M. O. F., & Emery, F. da S. (2020). Nitrosation of BODIPY dyes and their applications in the development of thiol sensors. Dyes and Pigments, 173, 1-7. doi:10.1016/j.dyepig.2019.107885

    • NLM

      Melo SMG de, Rezende LCD de, Petrilli R, Lopez RFV, Goulart MOF, Emery F da S. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors [Internet]. Dyes and Pigments. 2020 ; 173 1-7.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107885

    • Vancouver

      Melo SMG de, Rezende LCD de, Petrilli R, Lopez RFV, Goulart MOF, Emery F da S. Nitrosation of BODIPY dyes and their applications in the development of thiol sensors [Internet]. Dyes and Pigments. 2020 ; 173 1-7.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.dyepig.2019.107885

  • Artigo de periodico

    Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes (2019)

    González, María Teresa Páez; Mello, Shaiani Maria Gil de; Emery, Flavio da Silva

    Source: Journal of Fluorescence. Unidade: FCFRP

    Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS, CORANTES

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      GONZÁLEZ, María Teresa Páez e MELLO, Shaiani Maria Gil de e EMERY, Flavio da Silva. Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes. Journal of Fluorescence, v. 29, n. 4, p. 845-852, 2019Tradução . . Disponível em: https://doi.org/10.1007/s10895-019-02389-x. Acesso em: 27 nov. 2025.

    • APA

      González, M. T. P., Mello, S. M. G. de, & Emery, F. da S. (2019). Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes. Journal of Fluorescence, 29( 4), 845-852. doi:10.1007/s10895-019-02389-x

    • NLM

      González MTP, Mello SMG de, Emery F da S. Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes [Internet]. Journal of Fluorescence. 2019 ; 29( 4): 845-852.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1007/s10895-019-02389-x

    • Vancouver

      González MTP, Mello SMG de, Emery F da S. Influence of 1,3,5-triazine core and electron donor group in photophysical properties of BODIPY dyes [Internet]. Journal of Fluorescence. 2019 ; 29( 4): 845-852.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1007/s10895-019-02389-x

  • Artigo de periodico

    β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders (2018)

    Vaidergorn, Miguel M; Carneiro, Zumira A; Lopes, Carla D; Albuquerque, Sérgio de; Reis, Felipe C. C; Nikolaou, Sofia; Mello, Juliana F. R; Genesi, Giovani L; Trossini, Gustavo Henrique Goulart ; Ganesan, A; Emery, Flavio da Silva

    Source: European Journal of Medicinal Chemistry. Unidades: FCFRP, FFCLRP, FCF

    Subjects: DNA, COMPOSTOS ORGÂNICOS

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    • ABNT

      VAIDERGORN, Miguel M et al. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, v. 157, p. 657-664, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.07.055. Acesso em: 27 nov. 2025.

    • APA

      Vaidergorn, M. M., Carneiro, Z. A., Lopes, C. D., Albuquerque, S. de, Reis, F. C. C., Nikolaou, S., et al. (2018). β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, 157, 657-664. doi:10.1016/j.ejmech.2018.07.055

    • NLM

      Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055

    • Vancouver

      Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055

  • Artigo de periodico

    Understanding the fragmentation mechanisms of methoxy-, mesyl-, and tosyl-lapachol derivatives by computational chemistry and mass spectrometry analysis (2017)

    Vessecchi, Ricardo; Borges, Letícia da Silva; Emery, Flavio da Silva; Lopes, Norberto Peporine

    Source: International Journal of Mass Spectrometry. Unidades: FFCLRP, FCFRP

    Subjects: ESPECTROMETRIA DE MASSAS, COMPOSTOS ORGÂNICOS

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      VESSECCHI, Ricardo et al. Understanding the fragmentation mechanisms of methoxy-, mesyl-, and tosyl-lapachol derivatives by computational chemistry and mass spectrometry analysis. International Journal of Mass Spectrometry, v. 418, p. 92-100, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ijms.2016.11.012. Acesso em: 27 nov. 2025.

    • APA

      Vessecchi, R., Borges, L. da S., Emery, F. da S., & Lopes, N. P. (2017). Understanding the fragmentation mechanisms of methoxy-, mesyl-, and tosyl-lapachol derivatives by computational chemistry and mass spectrometry analysis. International Journal of Mass Spectrometry, 418, 92-100. doi:10.1016/j.ijms.2016.11.012

    • NLM

      Vessecchi R, Borges L da S, Emery F da S, Lopes NP. Understanding the fragmentation mechanisms of methoxy-, mesyl-, and tosyl-lapachol derivatives by computational chemistry and mass spectrometry analysis [Internet]. International Journal of Mass Spectrometry. 2017 ; 418 92-100.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.ijms.2016.11.012

    • Vancouver

      Vessecchi R, Borges L da S, Emery F da S, Lopes NP. Understanding the fragmentation mechanisms of methoxy-, mesyl-, and tosyl-lapachol derivatives by computational chemistry and mass spectrometry analysis [Internet]. International Journal of Mass Spectrometry. 2017 ; 418 92-100.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.ijms.2016.11.012

  • Artigo de periodico

    Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes (2016)

    Glowacka, Paulina C.; Maindron, Nicolas; Stephenson, G. Richard; Romieu, Anthony; Renard, Pierre-Yves; Emery, Flavio da Silva

    Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS

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      GLOWACKA, Paulina C. et al. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes. Tetrahedron Letters, v. 57, n. 45, p. 4991-4996, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.09.091. Acesso em: 27 nov. 2025.

    • APA

      Glowacka, P. C., Maindron, N., Stephenson, G. R., Romieu, A., Renard, P. -Y., & Emery, F. da S. (2016). Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes. Tetrahedron Letters, 57( 45), 4991-4996. doi:10.1016/j.tetlet.2016.09.091

    • NLM

      Glowacka PC, Maindron N, Stephenson GR, Romieu A, Renard P-Y, Emery F da S. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes [Internet]. Tetrahedron Letters. 2016 ; 57( 45): 4991-4996.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091

    • Vancouver

      Glowacka PC, Maindron N, Stephenson GR, Romieu A, Renard P-Y, Emery F da S. Synthesis and photophysical properties of iron-carbonyl complex–coumarin conjugates as potential bimodal IR–fluorescent probes [Internet]. Tetrahedron Letters. 2016 ; 57( 45): 4991-4996.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1016/j.tetlet.2016.09.091

  • Tese (Livre Docência)

    O processo evolutivo de biblioteca de compostos orgânicos: de quinonas à concepção de novos fragmentos heterocíclicos (2016)

    Emery, Flavio da Silva

    Unidade: FCFRP

    Subjects: COMPOSTOS ORGÂNICOS, PRODUTOS NATURAIS, BIBLIOTECAS, FÁRMACOS

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      EMERY, Flavio da Silva. O processo evolutivo de biblioteca de compostos orgânicos: de quinonas à concepção de novos fragmentos heterocíclicos. 2016. Tese (Livre Docência) – Universidade de São Paulo, Ribeirão Preto, 2016. . Acesso em: 27 nov. 2025.

    • APA

      Emery, F. da S. (2016). O processo evolutivo de biblioteca de compostos orgânicos: de quinonas à concepção de novos fragmentos heterocíclicos (Tese (Livre Docência). Universidade de São Paulo, Ribeirão Preto.

    • NLM

      Emery F da S. O processo evolutivo de biblioteca de compostos orgânicos: de quinonas à concepção de novos fragmentos heterocíclicos. 2016 ;[citado 2025 nov. 27 ]

    • Vancouver

      Emery F da S. O processo evolutivo de biblioteca de compostos orgânicos: de quinonas à concepção de novos fragmentos heterocíclicos. 2016 ;[citado 2025 nov. 27 ]

  • Artigo de periodico

    Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives (2015)

    Rezende, Lucas Cunha Dias de; Melo, Shaiani Maria Gil de; Boodts, Stijn; Verbelen, Bram; Dehaen, Wim; Emery, Flavio da Silva

    Source: Organic and Biomolecular Chemistry. Unidade: FCFRP

    Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS, CORANTES FLUORESCENTES

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      REZENDE, Lucas Cunha Dias de et al. Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives. Organic and Biomolecular Chemistry, v. 13, n. 21, p. 6031-6038, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5ob00499c. Acesso em: 27 nov. 2025.

    • APA

      Rezende, L. C. D. de, Melo, S. M. G. de, Boodts, S., Verbelen, B., Dehaen, W., & Emery, F. da S. (2015). Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives. Organic and Biomolecular Chemistry, 13( 21), 6031-6038. doi:10.1039/c5ob00499c

    • NLM

      Rezende LCD de, Melo SMG de, Boodts S, Verbelen B, Dehaen W, Emery F da S. Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives [Internet]. Organic and Biomolecular Chemistry. 2015 ; 13( 21): 6031-6038.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1039/c5ob00499c

    • Vancouver

      Rezende LCD de, Melo SMG de, Boodts S, Verbelen B, Dehaen W, Emery F da S. Thiocyanation of BODIPY dyes and their conversion to thioalkylated derivatives [Internet]. Organic and Biomolecular Chemistry. 2015 ; 13( 21): 6031-6038.[citado 2025 nov. 27 ] Available from: https://doi.org/10.1039/c5ob00499c
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