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Filtros : "Universidade Federal de São Carlos (UFSCar)" "FCF-FBF" Removido: "Leite, E. R." Limpar

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  • Artigo de periodico

    Controlled synthesis and structure characterization of a new fluconazole polymorph using analytical techniques and multivariate method (2024)

    Owoyemi, Bolaji Charles Dayo ; Silva, Cecília Carolina Pinheiro da ; Akinyemi, Amos Olalekan; Amuwaolorun, Banky Oluseye; Roque Flores, Roxana Lili; Araújo, Gabriel Lima Barros de ; Ellena, Javier ; Carneiro, Renato Lajarim

    Source: Scientific African. Unidades: IFSC, FCF

    Subjects: SOLUBILIDADE, ESPECTROSCOPIA RAMAN, POLIMORFISMO

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    • ABNT

      OWOYEMI, Bolaji Charles Dayo et al. Controlled synthesis and structure characterization of a new fluconazole polymorph using analytical techniques and multivariate method. Scientific African, v. 23, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.sciaf.2023.e02029. Acesso em: 15 jun. 2024.

    • APA

      Owoyemi, B. C. D., Silva, C. C. P. da, Akinyemi, A. O., Amuwaolorun, B. O., Roque Flores, R. L., Araújo, G. L. B. de, et al. (2024). Controlled synthesis and structure characterization of a new fluconazole polymorph using analytical techniques and multivariate method. Scientific African, 23. doi:10.1016/j.sciaf.2023.e02029

    • NLM

      Owoyemi BCD, Silva CCP da, Akinyemi AO, Amuwaolorun BO, Roque Flores RL, Araújo GLB de, Ellena J, Carneiro RL. Controlled synthesis and structure characterization of a new fluconazole polymorph using analytical techniques and multivariate method [Internet]. Scientific African. 2024 ; 23[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.sciaf.2023.e02029

    • Vancouver

      Owoyemi BCD, Silva CCP da, Akinyemi AO, Amuwaolorun BO, Roque Flores RL, Araújo GLB de, Ellena J, Carneiro RL. Controlled synthesis and structure characterization of a new fluconazole polymorph using analytical techniques and multivariate method [Internet]. Scientific African. 2024 ; 23[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.sciaf.2023.e02029

  • Artigo de periodico

    The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil (2023)

    Penteado, André Berndt ; Ribeiro, Geovani de Oliveira ; Araújo, Emerson Luiz Lima ; Kato, Rodrigo Bentes; Freire, Caio César de Melo ; Araújo, Joselio Maria Galvão de; Wallau, Gabriel da Luz; Salvato, Richard Steiner; Jesus, Ronaldo de; Bosco, Geraldine Goes ; Franz, Helena Ferreira; Silva, Pedro Eduardo Almeida da; Elcio de Souza Leal; Trossini, Gustavo Henrique Goulart ; Lima Neto, Daniel Ferreira de

    Source: Research Square. Unidades: FFCLRP, FCF

    Subjects: DENGUE, FILOGENIA

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      PENTEADO, André Berndt et al. The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil. Research Square, 2023Tradução . . Disponível em: https://doi.org/10.21203/rs.3.rs-3121559/v1. Acesso em: 15 jun. 2024.

    • APA

      Penteado, A. B., Ribeiro, G. de O., Araújo, E. L. L., Kato, R. B., Freire, C. C. de M., Araújo, J. M. G. de, et al. (2023). The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil. Research Square. doi:10.21203/rs.3.rs-3121559/v1

    • NLM

      Penteado AB, Ribeiro G de O, Araújo ELL, Kato RB, Freire CC de M, Araújo JMG de, Wallau G da L, Salvato RS, Jesus R de, Bosco GG, Franz HF, Silva PEA da, Elcio de Souza Leal, Trossini GHG, Lima Neto DF de. The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil [Internet]. Research Square. 2023 ;[citado 2024 jun. 15 ] Available from: https://doi.org/10.21203/rs.3.rs-3121559/v1

    • Vancouver

      Penteado AB, Ribeiro G de O, Araújo ELL, Kato RB, Freire CC de M, Araújo JMG de, Wallau G da L, Salvato RS, Jesus R de, Bosco GG, Franz HF, Silva PEA da, Elcio de Souza Leal, Trossini GHG, Lima Neto DF de. The Red Queen hypothesis from a structural perspective: a case study over 30 years of Dengue virus in Brazil [Internet]. Research Square. 2023 ;[citado 2024 jun. 15 ] Available from: https://doi.org/10.21203/rs.3.rs-3121559/v1

  • Artigo de periodico

    Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones (2019)

    Vasconcelos, Stanley Nunes Siqueira ; Oliveira, Isadora Maria de ; Shamim, Anwar ; Zukerman-Schpector, Júlio ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre

    Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC

    Subjects: ALDEÍDOS, ESTEREOQUÍMICA

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    • ABNT

      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: 15 jun. 2024.

    • APA

      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. 15 ] 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. 15 ] Available from: https://doi.org/10.1002/adsc.201900564

  • Artigo de periodico

    Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization (2019)

    Oliveira, Isadora M. de; Esteves, Carlos Henrique Alves ; Darbem, Mariana P; Pimenta, Daniel Carvalho ; Schpector, Júlio Zukerman ; Ferreira, Antônio Gilberto; Stefani, Hélio Alexandre ; Manarin, Flávia

    Source: Advanced Synthesis and Catalysis. Unidade: FCF

    Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO

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    • ABNT

      OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 15 jun. 2024.

    • APA

      Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142

    • NLM

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/adsc.201900142

    • Vancouver

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/adsc.201900142

  • Artigo de periodico

    Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling (2018)

    Oliveira, Isadora Maria de; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre ; Manarin, Flávia

    Source: New Journal of Chemistry. Unidade: FCF

    Subjects: SELÊNIO, ESTEREOQUÍMICA

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    • ABNT

      OLIVEIRA, Isadora Maria de et al. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, v. 42, n. 12, p. 10118-10123, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8nj01543k. Acesso em: 15 jun. 2024.

    • APA

      Oliveira, I. M. de, Pimenta, D. C., Zukerman-Schpector, J., Stefani, H. A., & Manarin, F. (2018). Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling. New Journal of Chemistry, 42( 12), 10118-10123. doi:10.1039/c8nj01543k

    • NLM

      Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1039/c8nj01543k

    • Vancouver

      Oliveira IM de, Pimenta DC, Zukerman-Schpector J, Stefani HA, Manarin F. Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling [Internet]. New Journal of Chemistry. 2018 ; 42( 12): 10118-10123.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1039/c8nj01543k

  • Artigo de periodico

    Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted (2018)

    Oliveira, Isadora M. de; Darbem, Mariana P; Esteves, Carlos Henrique Alves; Pimenta, Daniel C; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ITÉRBIO, SÍNTESE ORGÂNICA

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    • ABNT

      OLIVEIRA, Isadora M. de et al. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, v. 59, n. 24, p. 3907-3911, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.09.022. Acesso em: 15 jun. 2024.

    • APA

      Oliveira, I. M. de, Darbem, M. P., Esteves, C. H. A., Pimenta, D. C., Schpector, J. Z., Stefani, H. A., & Manarin, F. (2018). Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, 59( 24), 3907-3911. doi:10.1016/j.tetlet.2018.09.022

    • NLM

      Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022

    • Vancouver

      Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022

  • Artigo de periodico

    Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)

    Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre

    Source: Synthesis. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 15 jun. 2024.

    • APA

      Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090

    • NLM

      Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1055/s-0036-1589090

    • Vancouver

      Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1055/s-0036-1589090

  • Artigo de periodico

    Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles (2017)

    Vasconcelos, Stanley N. S; Fornari, Evelin; Caracelli, Ignez; Stefani, Hélio Alexandre

    Source: Molecular Diversity. Unidade: FCF

    Subjects: ALFA-AMINOÁCIDOS, SÍNTESE ORGÂNICA

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    • ABNT

      VASCONCELOS, Stanley N. S et al. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles. Molecular Diversity, v. 21, n. 4, p. 893-902, 2017Tradução . . Disponível em: https://doi.org/10.1007/s11030-017-9764-5. Acesso em: 15 jun. 2024.

    • APA

      Vasconcelos, S. N. S., Fornari, E., Caracelli, I., & Stefani, H. A. (2017). Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles. Molecular Diversity, 21( 4), 893-902. doi:10.1007/s11030-017-9764-5

    • NLM

      Vasconcelos SNS, Fornari E, Caracelli I, Stefani HA. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles [Internet]. Molecular Diversity. 2017 ; 21( 4): 893-902.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1007/s11030-017-9764-5

    • Vancouver

      Vasconcelos SNS, Fornari E, Caracelli I, Stefani HA. Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles [Internet]. Molecular Diversity. 2017 ; 21( 4): 893-902.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1007/s11030-017-9764-5

  • Artigo de periodico

    Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines (2017)

    Barbeiro, Cristiane de Souza; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Zukerman-Schpector, Júlio; Caracelli, Ignez; Maganhi, Stella Hernandez; Stefani, Hélio Alexandre

    Source: ChemistrySelect. Unidade: FCF

    Subjects: PALÁDIO, QUÍMICA FARMACÊUTICA

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    • ABNT

      BARBEIRO, Cristiane de Souza et al. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, v. 2, n. 26, p. 8173-8177, 2017Tradução . . Disponível em: https://doi.org/10.1002/slct.201701197. Acesso em: 15 jun. 2024.

    • APA

      Barbeiro, C. de S., Vasconcelos, S. N. S., Oliveira, I. M. de, Zukerman-Schpector, J., Caracelli, I., Maganhi, S. H., & Stefani, H. A. (2017). Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines. ChemistrySelect, 2( 26), 8173-8177. doi:10.1002/slct.201701197

    • NLM

      Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/slct.201701197

    • Vancouver

      Barbeiro C de S, Vasconcelos SNS, Oliveira IM de, Zukerman-Schpector J, Caracelli I, Maganhi SH, Stefani HA. Suzuki-Miyaura cross-coupling reaction catalyzed by palladium complexes of hydroxynaphthalene-2-oxazolines [Internet]. ChemistrySelect. 2017 ; 2( 26): 8173-8177.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/slct.201701197

  • Artigo de periodico

    Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles (2017)

    Ali, Bakhat; Vasconcelos, Stanley N. S; Shamim, Anwar; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre

    Source: Arabian Journal of Chemistry. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS

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      ALI, Bakhat et al. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, v. 10, n. 4, p. 500-508, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.06.003. Acesso em: 15 jun. 2024.

    • APA

      Ali, B., Vasconcelos, S. N. S., Shamim, A., Schpector, J. Z., & Stefani, H. A. (2017). Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, 10( 4), 500-508. doi:10.1016/j.arabjc.2016.06.003

    • NLM

      Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003

    • Vancouver

      Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003

  • Artigo de periodico

    Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines (2017)

    Oliveira, Isadora M. de; Vasconcelos, Stanley S. N; Barbeiro, Cristiane S; Correra, Thiago Carita ; Shamim, Anwar; Pimenta, Daniel Carvalho; Caracelli, Ignez; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia

    Source: New Journal of Chemistry. Unidades: IQ, FCF

    Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS

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      OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 15 jun. 2024.

    • APA

      Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g

    • NLM

      Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1039/c7nj01803g

    • Vancouver

      Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1039/c7nj01803g

  • Artigo de periodico

    Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis (2016)

    Schpector, Júlio Zukerman; Madureira, Lucas Sousa; Stefani, Hélio Alexandre ; Gozhina, Olga; Tiekink, Edward R. T

    Source: Zeitschrift fur Kristallographie. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, CRISTALOGRAFIA ESTRUTURAL

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    • ABNT

      SCHPECTOR, Júlio Zukerman et al. Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis. Zeitschrift fur Kristallographie, v. 231, n. 6, p. 329-339, 2016Tradução . . Disponível em: https://doi.org/10.1515/zkri-2015-1911. Acesso em: 15 jun. 2024.

    • APA

      Schpector, J. Z., Madureira, L. S., Stefani, H. A., Gozhina, O., & Tiekink, E. R. T. (2016). Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis. Zeitschrift fur Kristallographie, 231( 6), 329-339. doi:10.1515/zkri-2015-1911

    • NLM

      Schpector JZ, Madureira LS, Stefani HA, Gozhina O, Tiekink ERT. Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis [Internet]. Zeitschrift fur Kristallographie. 2016 ; 231( 6): 329-339.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1515/zkri-2015-1911

    • Vancouver

      Schpector JZ, Madureira LS, Stefani HA, Gozhina O, Tiekink ERT. Structural systematics of aryl-1,3-dithiane derivatives: crystal and energy-minimised structures, and Hirshfeld surface analysis [Internet]. Zeitschrift fur Kristallographie. 2016 ; 231( 6): 329-339.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1515/zkri-2015-1911

  • Artigo de periodico

    Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties (2016)

    Barbeiro, Cristiane S; Vasconcelos, Stanley Nunes Siqueira; Schpector, Júlio Zukerman; Caracelli, Ignez; Pimenta, Daniel C; Rodrigues, Ana Clara Beltran; Fernandes, André S; Correra, Thiago Carita ; Bastos, Erick Leite ; Stefani, Hélio Alexandre

    Source: ChemistrySelect. Unidades: IQ, FCF

    Subjects: MECANISMOS, FLUORESCÊNCIA

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    • ABNT

      BARBEIRO, Cristiane S et al. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, v. 2, p. 5647–5652, 2016Tradução . . Disponível em: https://doi.org/10.1002/slct.201601526. Acesso em: 15 jun. 2024.

    • APA

      Barbeiro, C. S., Vasconcelos, S. N. S., Schpector, J. Z., Caracelli, I., Pimenta, D. C., Rodrigues, A. C. B., et al. (2016). Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties. ChemistrySelect, 2, 5647–5652. doi:10.1002/slct.201601526

    • NLM

      Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/slct.201601526

    • Vancouver

      Barbeiro CS, Vasconcelos SNS, Schpector JZ, Caracelli I, Pimenta DC, Rodrigues ACB, Fernandes AS, Correra TC, Bastos EL, Stefani HA. Chlorinated 2-hydroxynaphthalenoxazolines: synthesis, reaction mechanism and fluorescence properties [Internet]. ChemistrySelect. 2016 ; 2 5647–5652.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/slct.201601526

  • Artigo de periodico

    Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound (2016)

    Caracelli, Ignez; Zukerman-Schpector, Júlio; Madureira, Lucas Sousa; Maganhi, Stella Hernandez; Stefani, Hélio Alexandre ; Guadagnin, Rafael C; Tiekink, Edward R. T

    Source: Zeitschrift fur Kristallographie - Crystalline Materials. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, COMPOSTOS ORGÂNICOS

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    • ABNT

      CARACELLI, Ignez et al. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound. Zeitschrift fur Kristallographie - Crystalline Materials, v. 231, n. 6, p. 321–328, 2016Tradução . . Disponível em: https://doi.org/10.1515/zkri-2016-1931. Acesso em: 15 jun. 2024.

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      Caracelli, I., Zukerman-Schpector, J., Madureira, L. S., Maganhi, S. H., Stefani, H. A., Guadagnin, R. C., & Tiekink, E. R. T. (2016). Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound. Zeitschrift fur Kristallographie - Crystalline Materials, 231( 6), 321–328. doi:10.1515/zkri-2016-1931

    • NLM

      Caracelli I, Zukerman-Schpector J, Madureira LS, Maganhi SH, Stefani HA, Guadagnin RC, Tiekink ERT. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound [Internet]. Zeitschrift fur Kristallographie - Crystalline Materials. 2016 ; 231( 6): 321–328.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1515/zkri-2016-1931

    • Vancouver

      Caracelli I, Zukerman-Schpector J, Madureira LS, Maganhi SH, Stefani HA, Guadagnin RC, Tiekink ERT. Crystallographic, DFT and docking (cathepsin B) studies on an organotellurium(IV) compound [Internet]. Zeitschrift fur Kristallographie - Crystalline Materials. 2016 ; 231( 6): 321–328.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1515/zkri-2016-1931

  • Artigo de periodico

    Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization (2015)

    Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Ali, Bakhat; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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    • ABNT

      SHAMIM, Anwar et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 15 jun. 2024.

    • APA

      Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052

    • NLM

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052

    • Vancouver

      Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052

  • Artigo de periodico

    Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes (2015)

    Ali, Bakhat; Schpector, Júlio Zukerman; Ferreira, Fernando P; Shamim, Anwar; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINAS, CATÁLISE

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    • ABNT

      ALI, Bakhat et al. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, v. 56, n. 9, p. 1153-1158, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 15 jun. 2024.

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      Ali, B., Schpector, J. Z., Ferreira, F. P., Shamim, A., Pimenta, D. C., & Stefani, H. A. (2015). Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, 56( 9), 1153-1158. doi:10.1016/j.tetlet.2015.01.059

    • NLM

      Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059

    • Vancouver

      Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059

  • Artigo de periodico

    Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers (2014)

    Schpector, Julio Zukermann; Madureira, Lucas Sousa; Wulf, Glaudeston Dutra; Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Ng, Seik Weng; Tiekink, Edward R. T

    Source: Molecules. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, SÍNTESE ORGÂNICA

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    • ABNT

      SCHPECTOR, Julio Zukermann et al. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, v. 19, n. 2, p. 1990-2003, 2014Tradução . . Disponível em: https://doi.org/10.3390/molecules19021990. Acesso em: 15 jun. 2024.

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      Schpector, J. Z., Madureira, L. S., Wulf, G. D., Stefani, H. A., Vasconcelos, S. N. S., Ng, S. W., & Tiekink, E. R. T. (2014). Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers. Molecules, 19( 2), 1990-2003. doi:10.3390/molecules19021990

    • NLM

      Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 jun. 15 ] Available from: https://doi.org/10.3390/molecules19021990

    • Vancouver

      Schpector JZ, Madureira LS, Wulf GD, Stefani HA, Vasconcelos SNS, Ng SW, Tiekink ERT. Synthesis, molecular and crystal structure analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT investigation of its rotational conformers [Internet]. Molecules. 2014 ; 19( 2): 1990-2003.[citado 2024 jun. 15 ] Available from: https://doi.org/10.3390/molecules19021990

  • Artigo de periodico

    N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin (2013)

    Maganhi, Stella Hernandez; Damião, Mariana Celestina Frojuello Bernstorff; Tavares, Maurício Temotheo; Parise Filho, Roberto

    Source: Acta Crystallographica Section E. Unidade: FCF

    Assunto: ANTINEOPLÁSICOS

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    • ABNT

      MAGANHI, Stella Hernandez et al. N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin. Acta Crystallographica Section E, v. E69, p. 0332 : + Supplementary materials ( S1-S6), 2013Tradução . . Disponível em: https://doi.org/10.1107/S1600536813002201. Acesso em: 15 jun. 2024.

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      Maganhi, S. H., Damião, M. C. F. B., Tavares, M. T., & Parise Filho, R. (2013). N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin. Acta Crystallographica Section E, E69, 0332 : + Supplementary materials ( S1-S6). doi:10.1107/S1600536813002201

    • NLM

      Maganhi SH, Damião MCFB, Tavares MT, Parise Filho R. N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin [Internet]. Acta Crystallographica Section E. 2013 ; E69 0332 : + Supplementary materials ( S1-S6).[citado 2024 jun. 15 ] Available from: https://doi.org/10.1107/S1600536813002201

    • Vancouver

      Maganhi SH, Damião MCFB, Tavares MT, Parise Filho R. N-[(1,3-Benzodioxol-5-yl)methyl]-4-methylbenzamide: an analogue of capsaicin [Internet]. Acta Crystallographica Section E. 2013 ; E69 0332 : + Supplementary materials ( S1-S6).[citado 2024 jun. 15 ] Available from: https://doi.org/10.1107/S1600536813002201

  • Artigo de periodico

    Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction (2013)

    Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Manarin, Flávia; Leal, Daiana Martins; Souza, Frederico B; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Eberlin, Marcos Nogueira; Godoi, Marla N; Galaverna, Renan de Souza

    Source: European Journal of Organic Chemistry. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, TELÚRIO

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    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction. European Journal of Organic Chemistry, n. 18, p. 3780-3783, 2013Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201300009. Acesso em: 15 jun. 2024.

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      Stefani, H. A., Vasconcelos, S. N. S., Manarin, F., Leal, D. M., Souza, F. B., Madureira, L. S., et al. (2013). Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction. European Journal of Organic Chemistry, ( 18), 3780-3783. doi:10.1002/ejoc.201300009

    • NLM

      Stefani HA, Vasconcelos SNS, Manarin F, Leal DM, Souza FB, Madureira LS, Zukerman-Schpector J, Eberlin MN, Godoi MN, Galaverna R de S. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction [Internet]. European Journal of Organic Chemistry. 2013 ;( 18): 3780-3783.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/ejoc.201300009

    • Vancouver

      Stefani HA, Vasconcelos SNS, Manarin F, Leal DM, Souza FB, Madureira LS, Zukerman-Schpector J, Eberlin MN, Godoi MN, Galaverna R de S. Synthesis of 5-organotellanyl-1H-1,2,3-triazoles: functionalization of the 5-position scaffold by the sonogashira cross-coupling reaction [Internet]. European Journal of Organic Chemistry. 2013 ;( 18): 3780-3783.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1002/ejoc.201300009

  • Artigo de periodico

    One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles (2013)

    Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Souza, Frederico B; Manarin, Flávia; Zukerman-Schpector, Júlio

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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    • ABNT

      STEFANI, Hélio Alexandre et al. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, v. 54, n. 43, p. 5821-5825, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.064. Acesso em: 15 jun. 2024.

    • APA

      Stefani, H. A., Vasconcelos, S. N. S., Souza, F. B., Manarin, F., & Zukerman-Schpector, J. (2013). One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, 54( 43), 5821-5825. doi:10.1016/j.tetlet.2013.08.064

    • NLM

      Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064

    • Vancouver

      Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 jun. 15 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064

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