Filtros : "FCF-FBF" "Alemanha" Removido: "Kedor-Hackmann, Erika Rosa Maria" Limpar

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  • Source: Brazilian Journal of Chemical Engineering. Unidade: FCF

    Subjects: MICROALGAS, CAROTENOIDES, BIOMASSA, MEIOS DE CULTURA

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      GOMES, Eleane de Almeida Cezare et al. Two-stage semi-continuous cultivation of Dunaliella salina for β-carotene production. Brazilian Journal of Chemical Engineering, v. 40, p. 367–378, 2023Tradução . . Disponível em: https://doi.org/10.1007/s43153-022-00246-2. Acesso em: 13 jun. 2024.
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      Gomes, E. de A. C., Lousada, M. E. G., Matsudo, M. C., Camargo, L. S. F., Ishii, M., Singh, A. K., & Carvalho, J. C. M. de. (2023). Two-stage semi-continuous cultivation of Dunaliella salina for β-carotene production. Brazilian Journal of Chemical Engineering, 40, 367–378. doi:10.1007/s43153-022-00246-2
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      Gomes E de AC, Lousada MEG, Matsudo MC, Camargo LSF, Ishii M, Singh AK, Carvalho JCM de. Two-stage semi-continuous cultivation of Dunaliella salina for β-carotene production [Internet]. Brazilian Journal of Chemical Engineering. 2023 ; 40 367–378.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s43153-022-00246-2
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      Gomes E de AC, Lousada MEG, Matsudo MC, Camargo LSF, Ishii M, Singh AK, Carvalho JCM de. Two-stage semi-continuous cultivation of Dunaliella salina for β-carotene production [Internet]. Brazilian Journal of Chemical Engineering. 2023 ; 40 367–378.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s43153-022-00246-2
  • Source: European Journal of Clinical Pharmacology. Unidade: FCF

    Subjects: PANDEMIAS, COVID-19, CORONAVIRUS

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      VAZ, Elisa Souza et al. Drug repositioning in the COVID-19 pandemic: fundamentals, synthetic routes, and overview of clinical studies. European Journal of Clinical Pharmacology, v. 79, p. 723–751, 2023Tradução . . Disponível em: https://doi.org/10.1007/s00228-023-03486-4. Acesso em: 13 jun. 2024.
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      Vaz, E. S., Vassiliades, S. V., Giarolla, J., Polli, M. C., & Parise Filho, R. (2023). Drug repositioning in the COVID-19 pandemic: fundamentals, synthetic routes, and overview of clinical studies. European Journal of Clinical Pharmacology, 79, 723–751. doi:10.1007/s00228-023-03486-4
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      Vaz ES, Vassiliades SV, Giarolla J, Polli MC, Parise Filho R. Drug repositioning in the COVID-19 pandemic: fundamentals, synthetic routes, and overview of clinical studies [Internet]. European Journal of Clinical Pharmacology. 2023 ; 79 723–751.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s00228-023-03486-4
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      Vaz ES, Vassiliades SV, Giarolla J, Polli MC, Parise Filho R. Drug repositioning in the COVID-19 pandemic: fundamentals, synthetic routes, and overview of clinical studies [Internet]. European Journal of Clinical Pharmacology. 2023 ; 79 723–751.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s00228-023-03486-4
  • Source: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Unidade: FCF

    Subjects: DESIGN, INDÚSTRIA FARMACÊUTICA

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      MAHR, Amanda Guiraldelli et al. Analytical Target Profile (ATP) and Method Operable Design Region (MODR). Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Tradução . Chaw: Springer, 2023. . . Acesso em: 13 jun. 2024.
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      Mahr, A. G., Lourenço, F. R., Borman, P., Weitzel, J., & Roussel, J. -M. (2023). Analytical Target Profile (ATP) and Method Operable Design Region (MODR). In Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Chaw: Springer.
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      Mahr AG, Lourenço FR, Borman P, Weitzel J, Roussel J-M. Analytical Target Profile (ATP) and Method Operable Design Region (MODR). In: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Chaw: Springer; 2023. [citado 2024 jun. 13 ]
    • Vancouver

      Mahr AG, Lourenço FR, Borman P, Weitzel J, Roussel J-M. Analytical Target Profile (ATP) and Method Operable Design Region (MODR). In: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Chaw: Springer; 2023. [citado 2024 jun. 13 ]
  • Source: Chemistry Select. Unidade: FCF

    Subjects: DOENÇA DE CHAGAS, DOENÇAS NEGLIGENCIADAS

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      PERNICHELLE, Filipe Gomes et al. The importance of the Piperazine ring for the development of trypanomicide compounds. Chemistry Select, v. 8, n. 33, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.1002/slct.202302697. Acesso em: 13 jun. 2024.
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      Pernichelle, F. G., Alves, E. T. M., Serafim, R. A. M., & Ferreira, E. I. (2023). The importance of the Piperazine ring for the development of trypanomicide compounds. Chemistry Select, 8( 33), 1-15. doi:10.1002/slct.202302697
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      Pernichelle FG, Alves ETM, Serafim RAM, Ferreira EI. The importance of the Piperazine ring for the development of trypanomicide compounds [Internet]. Chemistry Select. 2023 ; 8( 33): 1-15.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/slct.202302697
    • Vancouver

      Pernichelle FG, Alves ETM, Serafim RAM, Ferreira EI. The importance of the Piperazine ring for the development of trypanomicide compounds [Internet]. Chemistry Select. 2023 ; 8( 33): 1-15.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/slct.202302697
  • Source: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Unidade: FCF

    Subjects: DESIGN, INDÚSTRIA FARMACÊUTICA

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      MAHR, Amanda Guiraldelli et al. Analytical quality by design fundamentals and compendial and regulatory perspectives. Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Tradução . Chaw: Springer, 2023. . . Acesso em: 13 jun. 2024.
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      Mahr, A. G., Lourenço, F. R., Borman, P., Weitzel, J., & Roussel, J. -M. (2023). Analytical quality by design fundamentals and compendial and regulatory perspectives. In Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Chaw: Springer.
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      Mahr AG, Lourenço FR, Borman P, Weitzel J, Roussel J-M. Analytical quality by design fundamentals and compendial and regulatory perspectives. In: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Chaw: Springer; 2023. [citado 2024 jun. 13 ]
    • Vancouver

      Mahr AG, Lourenço FR, Borman P, Weitzel J, Roussel J-M. Analytical quality by design fundamentals and compendial and regulatory perspectives. In: Introduction to Quality by Design in Pharmaceutical Manufacturing and Analytical Development. Chaw: Springer; 2023. [citado 2024 jun. 13 ]
  • Source: Journal of the Korean Ceramic Society. Unidade: FCF

    Subjects: IMPRESSÃO 3-D, TERMOANÁLISE, FOSFATOS, CÁLCIO

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      LOPERA, Alex A et al. Obtaining a fused PLA-calcium phosphate-tobramycin-based filament for 3D printing with potential antimicrobial application. Journal of the Korean Ceramic Society, v. 60, n. 1, p. 169-182, 2023Tradução . . Disponível em: https://doi.org/10.1007/s43207-022-00255-4. Acesso em: 13 jun. 2024.
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      Lopera, A. A., Bezzon, V. D. N., Ospina, V., Castro, J. L. H., Ramirez, F. J., Ferraz, H. G., et al. (2023). Obtaining a fused PLA-calcium phosphate-tobramycin-based filament for 3D printing with potential antimicrobial application. Journal of the Korean Ceramic Society, 60( 1), 169-182. doi:10.1007/s43207-022-00255-4
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      Lopera AA, Bezzon VDN, Ospina V, Castro JLH, Ramirez FJ, Ferraz HG, Orlando MTA, Paucar CG, Robledo SM, Garcia CP. Obtaining a fused PLA-calcium phosphate-tobramycin-based filament for 3D printing with potential antimicrobial application [Internet]. Journal of the Korean Ceramic Society. 2023 ; 60( 1): 169-182.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s43207-022-00255-4
    • Vancouver

      Lopera AA, Bezzon VDN, Ospina V, Castro JLH, Ramirez FJ, Ferraz HG, Orlando MTA, Paucar CG, Robledo SM, Garcia CP. Obtaining a fused PLA-calcium phosphate-tobramycin-based filament for 3D printing with potential antimicrobial application [Internet]. Journal of the Korean Ceramic Society. 2023 ; 60( 1): 169-182.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s43207-022-00255-4
  • Source: Molecular informatics. Unidade: FCF

    Subjects: FÁRMACOS, ABSORÇÃO, BIODISPONIBILIDADE

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      TROSSINI, Gustavo Henrique Goulart et al. Absorption matters: a closer look at popular oral bioavailability rules for drug approvals. Molecular informatics, v. 42, n. 11, p. 1-12, 2023Tradução . . Disponível em: https://doi.org/10.1002/minf.202300115. Acesso em: 13 jun. 2024.
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      Trossini, G. H. G., Soares, A. C. G., Sousa, G. H. M., & Calil, R. L. (2023). Absorption matters: a closer look at popular oral bioavailability rules for drug approvals. Molecular informatics, 42( 11), 1-12. doi:10.1002/minf.202300115
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      Trossini GHG, Soares ACG, Sousa GHM, Calil RL. Absorption matters: a closer look at popular oral bioavailability rules for drug approvals [Internet]. Molecular informatics. 2023 ; 42( 11): 1-12.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/minf.202300115
    • Vancouver

      Trossini GHG, Soares ACG, Sousa GHM, Calil RL. Absorption matters: a closer look at popular oral bioavailability rules for drug approvals [Internet]. Molecular informatics. 2023 ; 42( 11): 1-12.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/minf.202300115
  • Source: Chromatographia. Unidades: IQ, FCF

    Subjects: ELETROFORESE CAPILAR DE ZONA, HIPERCOLESTEROLEMIA

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      SOUZA, Antonio Marcos Callejo de et al. Capillary electrophoresis method for simultaneous quantification of Hypocholesterolemic drugs in binary mixture formulation: fast, green, and cost-Effective Alternative to HPLC. Chromatographia, v. 86, p. 317–331, 2023Tradução . . Disponível em: https://doi.org/10.1007/s10337-023-04243-6. Acesso em: 13 jun. 2024.
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      Souza, A. M. C. de, Fajardo, F. A. G., Rashid, A., Tavares, M. F. M., & Aurora-Prado, M. S. (2023). Capillary electrophoresis method for simultaneous quantification of Hypocholesterolemic drugs in binary mixture formulation: fast, green, and cost-Effective Alternative to HPLC. Chromatographia, 86, 317–331. doi:10.1007/s10337-023-04243-6
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      Souza AMC de, Fajardo FAG, Rashid A, Tavares MFM, Aurora-Prado MS. Capillary electrophoresis method for simultaneous quantification of Hypocholesterolemic drugs in binary mixture formulation: fast, green, and cost-Effective Alternative to HPLC [Internet]. Chromatographia. 2023 ; 86 317–331.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s10337-023-04243-6
    • Vancouver

      Souza AMC de, Fajardo FAG, Rashid A, Tavares MFM, Aurora-Prado MS. Capillary electrophoresis method for simultaneous quantification of Hypocholesterolemic drugs in binary mixture formulation: fast, green, and cost-Effective Alternative to HPLC [Internet]. Chromatographia. 2023 ; 86 317–331.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s10337-023-04243-6
  • Source: European Journal of Organic Chemistry. Unidade: FCF

    Subjects: AMINOÁCIDOS, PROTEÍNAS, AMIDAS

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      JESUS, Jéssica Carol de et al. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, v. 2022, n. 30, p. 1-7 art. e202200332, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200332. Acesso em: 13 jun. 2024.
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      Jesus, J. C. de, Noguchi, H. K., Toledo, M. F. Z. J., Burrow, R. A., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, 2022( 30), 1-7 art. e202200332. doi:10.1002/ejoc.202200332
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      Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/ejoc.202200332
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      Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/ejoc.202200332
  • Source: European Journal of Clinical Pharmacology. Unidade: FCF

    Subjects: ANESTÉSICOS, REVISÃO SISTEMÁTICA, TRANSTORNOS MENTAIS, DEPRESSÃO

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      LIMA, Tácio de Mendonça e VISACRI, Marilia Berlofa e AGUIAR, Patrícia Melo. Use of ketamine and esketamine for depression: an overview of systematic reviews with meta-analyses. European Journal of Clinical Pharmacology, v. 78, p. 311-338, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00228-021-03216-8. Acesso em: 13 jun. 2024.
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      Lima, T. de M., Visacri, M. B., & Aguiar, P. M. (2022). Use of ketamine and esketamine for depression: an overview of systematic reviews with meta-analyses. European Journal of Clinical Pharmacology, 78, 311-338. doi:10.1007/s00228-021-03216-8
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      Lima T de M, Visacri MB, Aguiar PM. Use of ketamine and esketamine for depression: an overview of systematic reviews with meta-analyses [Internet]. European Journal of Clinical Pharmacology. 2022 ; 78 311-338.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s00228-021-03216-8
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      Lima T de M, Visacri MB, Aguiar PM. Use of ketamine and esketamine for depression: an overview of systematic reviews with meta-analyses [Internet]. European Journal of Clinical Pharmacology. 2022 ; 78 311-338.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1007/s00228-021-03216-8
  • Source: Scientific Reports. Unidade: FCF

    Subjects: NEOPLASIAS CEREBRAIS, QUIMIOTERAPIA, RADIOTERAPIA

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      RODRIGUES JUNIOR, Dorival Mendes et al. Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity. Scientific Reports, v. 12, p. 1-17, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-25534-2. Acesso em: 13 jun. 2024.
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      Rodrigues Junior, D. M., Raminelli, C., Hassanie, H., Trossini, G. H. G., Perecim, G. P., Puigsubira, L. C., et al. (2022). Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity. Scientific Reports, 12, 1-17. doi:10.1038/s41598-022-25534-2
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      Rodrigues Junior DM, Raminelli C, Hassanie H, Trossini GHG, Perecim GP, Puigsubira LC, Moustakas A, Vettore AL. Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity [Internet]. Scientific Reports. 2022 ; 12 1-17.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1038/s41598-022-25534-2
    • Vancouver

      Rodrigues Junior DM, Raminelli C, Hassanie H, Trossini GHG, Perecim GP, Puigsubira LC, Moustakas A, Vettore AL. Aporphine and isoquinoline derivatives block glioblastoma cell stemness and enhance temozolomide cytotoxicity [Internet]. Scientific Reports. 2022 ; 12 1-17.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1038/s41598-022-25534-2
  • Source: Journal of Separation Science. Unidade: FCF

    Subjects: FÁRMACOS IMUNOSSUPRESSORES, CARCINOGÊNESE

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      LIMA, Fabiana Vieira et al. Analytical tools for urocanic acid determination in human samples: a review. Journal of Separation Science, v. 44, n. 1, p. 438-447, 2021Tradução . . Disponível em: https://doi.org/10.1002/jssc.202000713. Acesso em: 13 jun. 2024.
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      Lima, F. V., Martins, T. E. A., Jacome, A. L. M., Almei, I. F., Rosado, C., Velasco, M. V. R., & Baby, A. R. (2021). Analytical tools for urocanic acid determination in human samples: a review. Journal of Separation Science, 44( 1), 438-447. doi:10.1002/jssc.202000713
    • NLM

      Lima FV, Martins TEA, Jacome ALM, Almei IF, Rosado C, Velasco MVR, Baby AR. Analytical tools for urocanic acid determination in human samples: a review [Internet]. Journal of Separation Science. 2021 ; 44( 1): 438-447.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/jssc.202000713
    • Vancouver

      Lima FV, Martins TEA, Jacome ALM, Almei IF, Rosado C, Velasco MVR, Baby AR. Analytical tools for urocanic acid determination in human samples: a review [Internet]. Journal of Separation Science. 2021 ; 44( 1): 438-447.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/jssc.202000713
  • Source: Molecular Informatics. Unidade: FCF

    Subjects: CORONAVIRUS, FÁRMACOS, COVID-19

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      FERNANDES, Mariana Sabo et al. Insights on 3D structures of potential drug-targeting proteins of SARS-CoV-2: application of cavity search and molecular docking. Molecular Informatics, v. 40, n. 2, p. 1-12, 2021Tradução . . Disponível em: https://doi.org/10.1002/minf.202000096. Acesso em: 13 jun. 2024.
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      Fernandes, M. S., Silva, F. S. da, Freitas, A. C. S. G., Melo, E. B. de, Trossini, G. H. G., & Paula, F. R. (2021). Insights on 3D structures of potential drug-targeting proteins of SARS-CoV-2: application of cavity search and molecular docking. Molecular Informatics, 40( 2), 1-12. doi:10.1002/minf.202000096
    • NLM

      Fernandes MS, Silva FS da, Freitas ACSG, Melo EB de, Trossini GHG, Paula FR. Insights on 3D structures of potential drug-targeting proteins of SARS-CoV-2: application of cavity search and molecular docking [Internet]. Molecular Informatics. 2021 ; 40( 2): 1-12.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/minf.202000096
    • Vancouver

      Fernandes MS, Silva FS da, Freitas ACSG, Melo EB de, Trossini GHG, Paula FR. Insights on 3D structures of potential drug-targeting proteins of SARS-CoV-2: application of cavity search and molecular docking [Internet]. Molecular Informatics. 2021 ; 40( 2): 1-12.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/minf.202000096
  • Source: European Journal of Organic Chemistry. Unidade: FCF

    Subjects: UREIA, PALÁDIO, GLICOCONJUGADOS

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      PAULINO, Antonio Augusto Soares e STEFANI, Hélio Alexandre. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 3847–3855, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000494. Acesso em: 13 jun. 2024.
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      Paulino, A. A. S., & Stefani, H. A. (2020). Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 3847–3855. doi:10.1002/ejoc.202000494
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      Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/ejoc.202000494
    • Vancouver

      Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/ejoc.202000494
  • Source: European Journal of Organic Chemistry. Unidades: FCF, IQ

    Subjects: GLICOSÍDEOS, PALÁDIO

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      DARBEM, Mariana P et al. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 5220–5226, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000846. Acesso em: 13 jun. 2024.
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      Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, & Stefani, H. A. (2020). α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 5220–5226. doi:10.1002/ejoc.202000846
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      Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/ejoc.202000846
    • Vancouver

      Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/ejoc.202000846
  • Source: European Physical Journal Special Topics. Unidades: FCF, IF

    Subjects: NÊUTRONS, RAIOS X, ANÁLISE TÉRMICA

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      LIMA, Cibele Rosana Ribeiro de Castro et al. Human hair: subtle change in the thioester groups dynamics observed by combining neutron scattering, X-ray diffraction and thermal analysis. European Physical Journal Special Topics, v. 229, p. 2825–2832, 2020Tradução . . Disponível em: https://doi.org/10.1140/epjst/e2020-900217-4. Acesso em: 13 jun. 2024.
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      Lima, C. R. R. de C., Lima, R. J. S., Machado, L. D. B., Velasco, M. V. R., Lakic, L., Nordentoft, M. S., et al. (2020). Human hair: subtle change in the thioester groups dynamics observed by combining neutron scattering, X-ray diffraction and thermal analysis. European Physical Journal Special Topics, 229, 2825–2832. doi:10.1140/epjst/e2020-900217-4
    • NLM

      Lima CRR de C, Lima RJS, Machado LDB, Velasco MVR, Lakic L, Nordentoft MS, Machuca-Beier L, Rudić S, Telling MTF, Sakai VG, Oliveira CLP de, Bordallo HN. Human hair: subtle change in the thioester groups dynamics observed by combining neutron scattering, X-ray diffraction and thermal analysis [Internet]. European Physical Journal Special Topics. 2020 ; 229 2825–2832.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1140/epjst/e2020-900217-4
    • Vancouver

      Lima CRR de C, Lima RJS, Machado LDB, Velasco MVR, Lakic L, Nordentoft MS, Machuca-Beier L, Rudić S, Telling MTF, Sakai VG, Oliveira CLP de, Bordallo HN. Human hair: subtle change in the thioester groups dynamics observed by combining neutron scattering, X-ray diffraction and thermal analysis [Internet]. European Physical Journal Special Topics. 2020 ; 229 2825–2832.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1140/epjst/e2020-900217-4
  • Source: ChemCatChem. Unidades: BIOTECNOLOGIA, FCF, IQ

    Subjects: PALÁDIO, HIDRÓLISE

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    • ABNT

      DARBEM, Mariana P et al. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, v. 12, n. 2, p. 576-583, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.201901403. Acesso em: 13 jun. 2024.
    • APA

      Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, Pimenta, D. C., & Stefani, H. A. (2020). Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, 12( 2), 576-583. doi:10.1002/cctc.201901403
    • NLM

      Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/cctc.201901403
    • Vancouver

      Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/cctc.201901403
  • Source: ChemCatChem. Unidades: FCF, IQ

    Subjects: LIGANTES, CATALISADORES

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      OLIVEIRA, Isadora Maria de et al. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, v. 12, p. 3545–3552, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.202000395. Acesso em: 13 jun. 2024.
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      Oliveira, I. M. de, Esteves, H. A., Darbem, M. P., Sartorelli, A., Correra, T. C., Oliveira, A. F. R., et al. (2020). Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, 12, 3545–3552. doi:10.1002/cctc.202000395
    • NLM

      Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/cctc.202000395
    • Vancouver

      Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/cctc.202000395
  • Source: European Journal of Pharmaceutics and Biopharmaceutics. Unidade: FCF

    Subjects: MATERIAIS NANOESTRUTURADOS, NEOPLASIAS

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      BARBOSA, Eduardo José et al. Niclosamide repositioning for treating cancer: Challenges and nano-based drug delivery opportunities. European Journal of Pharmaceutics and Biopharmaceutics, v. 141, p. 58-69, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.ejpb.2019.05.004. Acesso em: 13 jun. 2024.
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      Barbosa, E. J., Löbenberg, R., Araujo, G. L. B. de, & Bou-Chacra, N. A. (2019). Niclosamide repositioning for treating cancer: Challenges and nano-based drug delivery opportunities. European Journal of Pharmaceutics and Biopharmaceutics, 141, 58-69. doi:10.1016/j.ejpb.2019.05.004
    • NLM

      Barbosa EJ, Löbenberg R, Araujo GLB de, Bou-Chacra NA. Niclosamide repositioning for treating cancer: Challenges and nano-based drug delivery opportunities [Internet]. European Journal of Pharmaceutics and Biopharmaceutics. 2019 ; 141 58-69.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1016/j.ejpb.2019.05.004
    • Vancouver

      Barbosa EJ, Löbenberg R, Araujo GLB de, Bou-Chacra NA. Niclosamide repositioning for treating cancer: Challenges and nano-based drug delivery opportunities [Internet]. European Journal of Pharmaceutics and Biopharmaceutics. 2019 ; 141 58-69.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1016/j.ejpb.2019.05.004
  • Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC

    Subjects: ALDEÍDOS, ESTEREOQUÍMICA

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      VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 13 jun. 2024.
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      Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Pimenta, D. C., & Stefani, H. A. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564
    • NLM

      Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/adsc.201900564
    • Vancouver

      Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1002/adsc.201900564

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