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Artigo de periodico
Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides (2023)
Amaral, Alexandra A; Willig, Julia C. M; Olguin, Conceição F. A ; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre ; Botteselle, Giancarlo V ; Manarin, Flávia
Fonte: Journal of the Brazilian Chemical Society. Unidades: FCF, IQ
Assuntos: HERBICIDAS, FITOTOXICIDADE
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ABNT
AMARAL, Alexandra A et al. Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides. Journal of the Brazilian Chemical Society, v. 34, n. 10, p. 1464-1473, 2023Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20230058. Acesso em: 03 out. 2024.
APA
Amaral, A. A., Willig, J. C. M., Olguin, C. F. A., Oliveira, I. M. de, Stefani, H. A., Botteselle, G. V., & Manarin, F. (2023). Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides. Journal of the Brazilian Chemical Society, 34( 10), 1464-1473. doi:10.21577/0103-5053.20230058
NLM
Amaral AA, Willig JCM, Olguin CFA, Oliveira IM de, Stefani HA, Botteselle GV, Manarin F. Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides [Internet]. Journal of the Brazilian Chemical Society. 2023 ; 34( 10): 1464-1473.[citado 2024 out. 03 ] Available from: https://doi.org/10.21577/0103-5053.20230058
Vancouver
Amaral AA, Willig JCM, Olguin CFA, Oliveira IM de, Stefani HA, Botteselle GV, Manarin F. Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides [Internet]. Journal of the Brazilian Chemical Society. 2023 ; 34( 10): 1464-1473.[citado 2024 out. 03 ] Available from: https://doi.org/10.21577/0103-5053.20230058
Artigo de periodico
Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential (2020)
Costa, Claudia A; Lopes, Rayssa M; Ferraz, Letícia Silva; Esteves, Gabriela N. N; Di Iorio, Juliana F; Souza, Aline A; Oliveira, Isadora M. de; Manarin, Flávia ; Judice, Wagner Alves de Souza; Stefani, Hélio Alexandre ; Rodrigues, Tiago
Fonte: Bioorganic & Medicinal Chemistry. Unidade: FCF
Assuntos: ANTINEOPLÁSICOS, ANTIPROTOZOÁRIOS, APOPTOSE
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ABNT
COSTA, Claudia A et al. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, v. 28, p. 1-13 art. 115511, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115511. Acesso em: 03 out. 2024.
APA
Costa, C. A., Lopes, R. M., Ferraz, L. S., Esteves, G. N. N., Di Iorio, J. F., Souza, A. A., et al. (2020). Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, 28, 1-13 art. 115511. doi:10.1016/j.bmc.2020.115511
NLM
Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
Vancouver
Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
Artigo de periodico
A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions (2020)
Willing, Julia C. Mansano; Granetto, Gustavo; Reginato, Danielly; Dutra, Felipe R; Poruczinski, Erica Fernanda; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre ; de Campos, Silvia D; Campos, Elvio A. de; Manarin, Flávia ; Botteselle, Giancarlo, V
Fonte: RSC Advances. Unidade: FCF
Assuntos: CATÁLISE, COBRE
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ABNT
WILLING, Julia C. Mansano et al. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions. RSC Advances, v. 10, n. 6, p. 3407-3415, 2020Tradução . . Disponível em: https://doi.org/10.1039/c9ra10171c. Acesso em: 03 out. 2024.
APA
Willing, J. C. M., Granetto, G., Reginato, D., Dutra, F. R., Poruczinski, E. F., Oliveira, I. M. de, et al. (2020). A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions. RSC Advances, 10( 6), 3407-3415. doi:10.1039/c9ra10171c
NLM
Willing JCM, Granetto G, Reginato D, Dutra FR, Poruczinski EF, Oliveira IM de, Stefani HA, de Campos SD, Campos EA de, Manarin F, Botteselle G. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions [Internet]. RSC Advances. 2020 ; 10( 6): 3407-3415.[citado 2024 out. 03 ] Available from: https://doi.org/10.1039/c9ra10171c
Vancouver
Willing JCM, Granetto G, Reginato D, Dutra FR, Poruczinski EF, Oliveira IM de, Stefani HA, de Campos SD, Campos EA de, Manarin F, Botteselle G. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions [Internet]. RSC Advances. 2020 ; 10( 6): 3407-3415.[citado 2024 out. 03 ] Available from: https://doi.org/10.1039/c9ra10171c
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
Fonte: Advanced Synthesis and Catalysis. Unidade: FCF
Assuntos: 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: 03 out. 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 out. 03 ] 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 out. 03 ] Available from: https://doi.org/10.1002/adsc.201900142
Trabalho de evento
Identificação de novos antimicrobianos derivados de 4-organoseleno-quinolinas contra bactéria Staphyloccocus aureus (2019)
Santos, Milena Noronha dos; Wiggers, Helton José; Cheleski, Juliana; Manarin, Flávia ; Moraes, L. A; Stefani, Hélio Alexandre ; Oliveira, Isadora Maria de
Fonte: Anais. Nome do evento: Congresso Brasileiro de Química/CBQ. Unidade: FCF
Assunto: ANTIBIÓTICOS
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ABNT
SANTOS, Milena Noronha dos et al. Identificação de novos antimicrobianos derivados de 4-organoseleno-quinolinas contra bactéria Staphyloccocus aureus. 2019, Anais.. Rio de Janeiro: Associação Brasileira de Química/ABQ, 2019. Disponível em: https://www.abq.org.br/cbq/trabalhos_aceitos_detalhes,1678.html. Acesso em: 03 out. 2024.
APA
Santos, M. N. dos, Wiggers, H. J., Cheleski, J., Manarin, F., Moraes, L. A., Stefani, H. A., & Oliveira, I. M. de. (2019). Identificação de novos antimicrobianos derivados de 4-organoseleno-quinolinas contra bactéria Staphyloccocus aureus. In Anais. Rio de Janeiro: Associação Brasileira de Química/ABQ. Recuperado de https://www.abq.org.br/cbq/trabalhos_aceitos_detalhes,1678.html
NLM
Santos MN dos, Wiggers HJ, Cheleski J, Manarin F, Moraes LA, Stefani HA, Oliveira IM de. Identificação de novos antimicrobianos derivados de 4-organoseleno-quinolinas contra bactéria Staphyloccocus aureus [Internet]. Anais. 2019 ;[citado 2024 out. 03 ] Available from: https://www.abq.org.br/cbq/trabalhos_aceitos_detalhes,1678.html
Vancouver
Santos MN dos, Wiggers HJ, Cheleski J, Manarin F, Moraes LA, Stefani HA, Oliveira IM de. Identificação de novos antimicrobianos derivados de 4-organoseleno-quinolinas contra bactéria Staphyloccocus aureus [Internet]. Anais. 2019 ;[citado 2024 out. 03 ] Available from: https://www.abq.org.br/cbq/trabalhos_aceitos_detalhes,1678.html
Artigo de periodico
Síntese de bis(indolil)metanos utilizando Fe3O4 nanoparticulado como um catalisador robusto, eficiente e recuperável magneticamente sob condição livre de solvente (2018)
Willig, Julia Caroline Manzano; Amaral, Alexandra A; Rafique, Jamal; Saba, Sumbal; Valiati, Stefany; Oliveira, Isadora Maria de; Stefani, Hélio Alexandre ; Manarin, Flávia; Botteselle, Giancarlo V
Fonte: Revista Virtual de Química. Unidade: FCF
Assuntos: CATÁLISE, ALQUILAÇÃO
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ABNT
WILLIG, Julia Caroline Manzano et al. Síntese de bis(indolil)metanos utilizando Fe3O4 nanoparticulado como um catalisador robusto, eficiente e recuperável magneticamente sob condição livre de solvente. Revista Virtual de Química, v. 10, n. 5, p. 1591-1606, 2018Tradução . . Disponível em: https://doi.org/10.21577/1984-6835.20180108. Acesso em: 03 out. 2024.
APA
Willig, J. C. M., Amaral, A. A., Rafique, J., Saba, S., Valiati, S., Oliveira, I. M. de, et al. (2018). Síntese de bis(indolil)metanos utilizando Fe3O4 nanoparticulado como um catalisador robusto, eficiente e recuperável magneticamente sob condição livre de solvente. Revista Virtual de Química, 10( 5), 1591-1606. doi:10.21577/1984-6835.20180108
NLM
Willig JCM, Amaral AA, Rafique J, Saba S, Valiati S, Oliveira IM de, Stefani HA, Manarin F, Botteselle GV. Síntese de bis(indolil)metanos utilizando Fe3O4 nanoparticulado como um catalisador robusto, eficiente e recuperável magneticamente sob condição livre de solvente [Internet]. Revista Virtual de Química. 2018 ; 10( 5): 1591-1606.[citado 2024 out. 03 ] Available from: https://doi.org/10.21577/1984-6835.20180108
Vancouver
Willig JCM, Amaral AA, Rafique J, Saba S, Valiati S, Oliveira IM de, Stefani HA, Manarin F, Botteselle GV. Síntese de bis(indolil)metanos utilizando Fe3O4 nanoparticulado como um catalisador robusto, eficiente e recuperável magneticamente sob condição livre de solvente [Internet]. Revista Virtual de Química. 2018 ; 10( 5): 1591-1606.[citado 2024 out. 03 ] Available from: https://doi.org/10.21577/1984-6835.20180108
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
Fonte: New Journal of Chemistry. Unidade: FCF
Assuntos: 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: 03 out. 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 out. 03 ] 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 out. 03 ] Available from: https://doi.org/10.1039/c8nj01543k
Artigo de periodico
Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) (2018)
Tornquist, Bruna Luisa; Bueno, Gabriel de Paula; Willig, Julia Caroline Manzano; Oliveira, Isadora Maria de; Stefani, Hélio Alexandre ; Rafique, Jamal; Saba, Sumbal; Iglesias, Bernardo Almeida; Botteselle, Giancarlo V; Manarin, Flávia
Fonte: ChemistrySelect. Unidade: FCF
Assuntos: ITÉRBIO, SÓDIO
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ABNT
TORNQUIST, Bruna Luisa et al. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs). ChemistrySelect, v. 3, p. 6358-6363, 2018Tradução . . Disponível em: https://doi.org/10.1002/slct.201800673. Acesso em: 03 out. 2024.
APA
Tornquist, B. L., Bueno, G. de P., Willig, J. C. M., Oliveira, I. M. de, Stefani, H. A., Rafique, J., et al. (2018). Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs). ChemistrySelect, 3, 6358-6363. doi:10.1002/slct.201800673
NLM
Tornquist BL, Bueno G de P, Willig JCM, Oliveira IM de, Stefani HA, Rafique J, Saba S, Iglesias BA, Botteselle GV, Manarin F. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) [Internet]. ChemistrySelect. 2018 ; 3 6358-6363.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/slct.201800673
Vancouver
Tornquist BL, Bueno G de P, Willig JCM, Oliveira IM de, Stefani HA, Rafique J, Saba S, Iglesias BA, Botteselle GV, Manarin F. Ytterbium (III) triflate/sodium dodecyl sulfate: a versatile recyclable and water-tolerant catalyst for the synthesis of bis(indolyl)methanes (BIMs) [Internet]. ChemistrySelect. 2018 ; 3 6358-6363.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/slct.201800673
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
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: 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: 03 out. 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 out. 03 ] 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 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Trabalho de evento-resumo
Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction (2017)
Oliveira, Isadora Maria de; Stefani, Hélio Alexandre ; Manarin, Flávia
Fonte: Proceedings. Nome do evento: World Chemistry Congress. Unidade: FCF
Assuntos: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
OLIVEIRA, Isadora Maria de e STEFANI, Hélio Alexandre e MANARIN, Flávia. Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 03 out. 2024.
APA
Oliveira, I. M. de, Stefani, H. A., & Manarin, F. (2017). Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Oliveira IM de, Stefani HA, Manarin F. Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction [Internet]. Proceedings. 2017 ;[citado 2024 out. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Oliveira IM de, Stefani HA, Manarin F. Synthesis of 4-organoselenium-quinolines via povarov reaction: application in the copper-free sonogashira cross-coupling reaction [Internet]. Proceedings. 2017 ;[citado 2024 out. 03 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
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
Fonte: New Journal of Chemistry. Unidades: IQ, FCF
Assuntos: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
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: 03 out. 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 out. 03 ] 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 out. 03 ] Available from: https://doi.org/10.1039/c7nj01803g
Artigo de periodico
Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters (2014)
Stefani, Hélio Alexandre ; Manarin, Flávia; Khan, Amna N; Vasconcelos, Stanley Nunes Siqueira
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: ITÉRBIO, BORO, SÍNTESE ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, v. 6, p. 1236-1240, 2014Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201301421. Acesso em: 03 out. 2024.
APA
Stefani, H. A., Manarin, F., Khan, A. N., & Vasconcelos, S. N. S. (2014). Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters. European Journal of Organic Chemistry, 6, 1236-1240. doi:10.1002/ejoc.201301421
NLM
Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ejoc.201301421
Vancouver
Stefani HA, Manarin F, Khan AN, Vasconcelos SNS. Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters: efficient synthesis of β-unsaturated α-amino esters [Internet]. European Journal of Organic Chemistry. 2014 ; 6 1236-1240.[citado 2024 out. 03 ] Available from: https://doi.org/10.1002/ejoc.201301421
Artigo de periodico
Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters (2014)
Stefani, Hélio Alexandre ; Manarin, Flávia; Sousa, Ariane C.S; Souza, Frederico B; Ferraz, Witor Ribeiro
Fonte: Tetrahedron. Unidade: FCF
Assuntos: ITÉRBIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, v. 70, n. 20, p. 3243-3248, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.11.107. Acesso em: 03 out. 2024.
APA
Stefani, H. A., Manarin, F., Sousa, A. C. S., Souza, F. B., & Ferraz, W. R. (2014). Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, 70( 20), 3243-3248. doi:10.1016/j.tet.2013.11.107
NLM
Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tet.2013.11.107
Vancouver
Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tet.2013.11.107
Artigo de periodico
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction (2013)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Vasconcelos, Stanley Nunes Siqueira; Manarin, Flávia; Souza, Frederico B
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: TELÚRIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, v. 54, n. 22, p. 2809-2812, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.03.061. Acesso em: 03 out. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Vasconcelos, S. N. S., Manarin, F., & Souza, F. B. (2013). Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, 54( 22), 2809-2812. doi:10.1016/j.tetlet.2013.03.061
NLM
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
Vancouver
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
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
Fonte: European Journal of Organic Chemistry. Unidade: FCF
Assuntos: COMPOSTOS HETEROCÍCLICOS, TELÚRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 out. 2024.
APA
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 out. 03 ] 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 out. 03 ] 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
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 03 out. 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 out. 03 ] 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 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
Artigo de periodico
Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ (2013)
Stefani, Hélio Alexandre ; Khan, AMNA N; Manarin, Flávia; Vendramini, Pedro H; Eberlin, Marcos Nogueira
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: AMINOÁCIDOS, ITÉRBIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´. Tetrahedron Letters, v. 54, n. 46, p. 6204-6207, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.133. Acesso em: 03 out. 2024.
APA
Stefani, H. A., Khan, A. M. N. A. N., Manarin, F., Vendramini, P. H., & Eberlin, M. N. (2013). Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´. Tetrahedron Letters, 54( 46), 6204-6207. doi:10.1016/j.tetlet.2013.08.133
NLM
Stefani HA, Khan AMNAN, Manarin F, Vendramini PH, Eberlin MN. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ [Internet]. Tetrahedron Letters. 2013 ; 54( 46): 6204-6207.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.133
Vancouver
Stefani HA, Khan AMNAN, Manarin F, Vendramini PH, Eberlin MN. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ [Internet]. Tetrahedron Letters. 2013 ; 54( 46): 6204-6207.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.133
Artigo de periodico
Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction (2012)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Manarin, Flávia; Lüdtke, Diogo, Seibert; Zukerman-Schpector, Júlio; Madureira, Lucas Sousa; Tiekink, Edward R. T
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, v. 53, n. 14, p. 1742-1747 : + Supplementary materials ( S1-S36), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.01.102. Acesso em: 03 out. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Manarin, F., Lüdtke, D., Zukerman-Schpector, J., Madureira, L. S., & Tiekink, E. R. T. (2012). Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, 53( 14), 1742-1747 : + Supplementary materials ( S1-S36). doi:10.1016/j.tetlet.2012.01.102
NLM
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Vancouver
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Artigo de periodico
Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: effect on inducible nitric oxide synthase (2012)
Stefani, Hélio Alexandre ; Gueogjan, Karina; Manarin, Flávia; Farsky, Sandra Helena Poliselli ; Zukerman-Schpector, Julio; Caracelli, Ignez; Rodrigues, Sergio R. Pizano; Muscará, Marcelo Nicolás ; Teixeira, Simone Aparecida; Santin, José R; Machado, Isabel D; Bolonheis, Simone M; Curi, Rui; Vinolo, Marco Aurelio Ramirez
Fonte: European Journal of Medicinal Chemistry. Unidades: ICB, FCF
Assuntos: FISIOLOGIA, FARMACOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: effect on inducible nitric oxide synthase. European Journal of Medicinal Chemistry, v. 58, p. 117-127, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2012.10.010. Acesso em: 03 out. 2024.
APA
Stefani, H. A., Gueogjan, K., Manarin, F., Farsky, S. H. P., Zukerman-Schpector, J., Caracelli, I., et al. (2012). Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: effect on inducible nitric oxide synthase. European Journal of Medicinal Chemistry, 58, 117-127. doi:10.1016/j.ejmech.2012.10.010
NLM
Stefani HA, Gueogjan K, Manarin F, Farsky SHP, Zukerman-Schpector J, Caracelli I, Rodrigues SRP, Muscará MN, Teixeira SA, Santin JR, Machado ID, Bolonheis SM, Curi R, Vinolo MAR. Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: effect on inducible nitric oxide synthase [Internet]. European Journal of Medicinal Chemistry. 2012 ; 58 117-127.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2012.10.010
Vancouver
Stefani HA, Gueogjan K, Manarin F, Farsky SHP, Zukerman-Schpector J, Caracelli I, Rodrigues SRP, Muscará MN, Teixeira SA, Santin JR, Machado ID, Bolonheis SM, Curi R, Vinolo MAR. Synthesis, biological evaluation and molecular docking studies of 3-(triazolyl)-coumarin derivatives: effect on inducible nitric oxide synthase [Internet]. European Journal of Medicinal Chemistry. 2012 ; 58 117-127.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejmech.2012.10.010
Artigo de periodico
Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions (2011)
Stefani, Hélio Alexandre ; Amaral, Mônica Franco Zannini Junqueira; Manarin, Flávia; Ando, Rômulo Augusto ; Silva, Nathalia Cristina S; Juaristi, Eusebio
Fonte: Tetrahedron Letters. Unidades: FCF, IQ
Assuntos: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, v. 52, n. 51, p. 6883-6886 : + Supplementary materials ( S1-S6), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.10.011. Acesso em: 03 out. 2024.
APA
Stefani, H. A., Amaral, M. F. Z. J., Manarin, F., Ando, R. A., Silva, N. C. S., & Juaristi, E. (2011). Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, 52( 51), 6883-6886 : + Supplementary materials ( S1-S6). doi:10.1016/j.tetlet.2011.10.011
NLM
Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
Vancouver
Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011

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