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Filtros : "STEFANI, HELIO ALEXANDRE" "Reino Unido" Removido: "Financiado pela EMBRAPA" Limpar

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  • 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

    Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511

  • Artigo de periodico

    Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor (2020)

    Paulino, Antonio Augusto Soares; Giroldo, Lilian; Pradie, Noriberto Araújo; Reis, Joel Savi dos; Back, Davi F; Braga, Ataualpa Albert Carmo ; Stefani, Hélio Alexandre ; Lodeiro, Carlos; Santos, Alcindo Aparecido dos

    Source: Dyes and Pigments. Unidades: IQ, FCF

    Subjects: SELÊNIO, PALÁDIO, FLUORESCÊNCIA

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      PAULINO, Antonio Augusto Soares et al. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, v. 179, p. 1-10 art. 108355, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108355. Acesso em: 28 jun. 2024.

    • APA

      Paulino, A. A. S., Giroldo, L., Pradie, N. A., Reis, J. S. dos, Back, D. F., Braga, A. A. C., et al. (2020). Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, 179, 1-10 art. 108355. doi:10.1016/j.dyepig.2020.108355

    • NLM

      Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355

    • Vancouver

      Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355

  • Artigo de periodico

    Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution (2019)

    Santos, Fabiano S; Zanotto, Gabriel M; Argomedo, Luiz M. Z; Darbem, Mariana P; Gonçalves, Paulo F. B; Stefani, Hélio Alexandre ; Rodembusch, Fabiano S

    Source: Dyes and Pigments. Unidade: FCF

    Subjects: SENSORES ÓPTICOS, SÍNTESE ORGÂNICA

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      SANTOS, Fabiano S et al. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, v. 165, p. 372-382, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.02.047. Acesso em: 28 jun. 2024.

    • APA

      Santos, F. S., Zanotto, G. M., Argomedo, L. M. Z., Darbem, M. P., Gonçalves, P. F. B., Stefani, H. A., & Rodembusch, F. S. (2019). Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, 165, 372-382. doi:10.1016/j.dyepig.2019.02.047

    • NLM

      Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047

    • Vancouver

      Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047

  • Artigo de periodico

    Synthesis of symmetrical biaryl compounds by homocoupling reaction (2019)

    Vasconcelos, Stanley N. S; Reis, Joel S; Oliveira, Isadora M. de; Balfour, Michael N; Stefani, Hélio Alexandre

    Source: Tetrahedron. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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    • ABNT

      VASCONCELOS, Stanley N. S et al. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, v. 75, p. 1865-1959, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2019.02.001. Acesso em: 28 jun. 2024.

    • APA

      Vasconcelos, S. N. S., Reis, J. S., Oliveira, I. M. de, Balfour, M. N., & Stefani, H. A. (2019). Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, 75, 1865-1959. doi:10.1016/j.tet.2019.02.001

    • NLM

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001

    • Vancouver

      Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001

  • Artigo de periodico

    Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum (2019)

    Vasconcelos, Stanley Nunes Siqueira ; Meissner, Kamila Anna ; Ferraz, Witor R.; Trossini, Gustavo Henrique Goulart ; Wrenger, Carsten ; Stefani, Hélio Alexandre

    Source: Future Medicinal Chemistry. Unidades: FCF, ICB

    Subjects: MALÁRIA, PLASMODIUM FALCIPARUM, PROTOZOA, ANTIMALÁRICOS, ANIMAIS PARASITOS, VIRULÊNCIA

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    • ABNT

      VASCONCELOS, Stanley Nunes Siqueira et al. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum. Future Medicinal Chemistry, v. 11, n. 6, p. 525-538, 2019Tradução . . Disponível em: https://doi.org/10.4155/fmc-2018-0246. Acesso em: 28 jun. 2024.

    • APA

      Vasconcelos, S. N. S., Meissner, K. A., Ferraz, W. R., Trossini, G. H. G., Wrenger, C., & Stefani, H. A. (2019). Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum. Future Medicinal Chemistry, 11( 6), 525-538. doi:10.4155/fmc-2018-0246

    • NLM

      Vasconcelos SNS, Meissner KA, Ferraz WR, Trossini GHG, Wrenger C, Stefani HA. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum [Internet]. Future Medicinal Chemistry. 2019 ; 11( 6): 525-538.[citado 2024 jun. 28 ] Available from: https://doi.org/10.4155/fmc-2018-0246

    • Vancouver

      Vasconcelos SNS, Meissner KA, Ferraz WR, Trossini GHG, Wrenger C, Stefani HA. Indole-3-glyoxyl tyrosine: synthesis and antimalarial activity against Plasmodium falciparum [Internet]. Future Medicinal Chemistry. 2019 ; 11( 6): 525-538.[citado 2024 jun. 28 ] Available from: https://doi.org/10.4155/fmc-2018-0246

  • Artigo de periodico

    Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction (2019)

    Darbem, Mariana P; Esteves, C. Henrique A; Oliveira, Isadora M. de; Reis, Joel S; Pimenta, Daniel C; Stefani, Hélio Alexandre

    Source: RSC Advances. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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    • ABNT

      DARBEM, Mariana P et al. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, v. 9, p. 9468–9474, 2019Tradução . . Disponível em: https://doi.org/10.1039/c9ra00523d. Acesso em: 28 jun. 2024.

    • APA

      Darbem, M. P., Esteves, C. H. A., Oliveira, I. M. de, Reis, J. S., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction. RSC Advances, 9, 9468–9474. doi:10.1039/c9ra00523d

    • NLM

      Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1039/c9ra00523d

    • Vancouver

      Darbem MP, Esteves CHA, Oliveira IM de, Reis JS, Pimenta DC, Stefani HA. Synthesis of D-glyco-alkynone derivatives via carbonylative Sonogashira reaction [Internet]. RSC Advances. 2019 ; 9 9468–9474.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1039/c9ra00523d

  • Artigo de periodico

    Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source (2019)

    Darbem, Mariana P; Kanno, Karina S; Oliveira, Isadora M. de; Esteves, C. Henrique A; Pimenta, Daniel C; Stefani, Hélio Alexandre

    Source: New Journal of Chemistry. Unidade: FCF

    Subjects: MONÓXIDO DE CARBONO, MOLIBDÊNIO

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    • ABNT

      DARBEM, Mariana P et al. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, v. 43, n. 2, p. 696-699, 2019Tradução . . Disponível em: https://doi.org/10.1039/c8nj04540b. Acesso em: 28 jun. 2024.

    • APA

      Darbem, M. P., Kanno, K. S., Oliveira, I. M. de, Esteves, C. H. A., Pimenta, D. C., & Stefani, H. A. (2019). Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source. New Journal of Chemistry, 43( 2), 696-699. doi:10.1039/c8nj04540b

    • NLM

      Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1039/c8nj04540b

    • Vancouver

      Darbem MP, Kanno KS, Oliveira IM de, Esteves CHA, Pimenta DC, Stefani HA. Synthesis of amidoglucals and glucal esters via carbonylative coupling reactions of 2-iodoglucal using Mo(CO)(6) as a CO source [Internet]. New Journal of Chemistry. 2019 ; 43( 2): 696-699.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1039/c8nj04540b

  • Artigo de periodico

    Oxazoline as acceptor moiety for excited-state intramolecular proton transfer (2018)

    Reis, Joel S; Fernandes, Arthur Bonfá; Dörr, Barbara Coelho de Freitas; Bastos, Erick Leite ; Stefani, Hélio Alexandre

    Source: Tetrahedron. Unidades: IQ, FCF

    Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS

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      REIS, Joel S et al. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, v. 74, p. 6866-6872, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2018.10.019. Acesso em: 28 jun. 2024.

    • APA

      Reis, J. S., Fernandes, A. B., Dörr, B. C. de F., Bastos, E. L., & Stefani, H. A. (2018). Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, 74, 6866-6872. doi:10.1016/j.tet.2018.10.019

    • NLM

      Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019

    • Vancouver

      Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019

  • 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: 28 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. 28 ] 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. 28 ] 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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      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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022

  • Artigo de periodico

    Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization (2017)

    Shamim, Anwar; Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, COBRE

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      SHAMIM, Anwar et al. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, v. 58, n. 9, p. 884-888, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.059. Acesso em: 28 jun. 2024.

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      Shamim, A., Souza, F. B. de, Vasconcelos, S. N. S., & Stefani, H. A. (2017). Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, 58( 9), 884-888. doi:10.1016/j.tetlet.2017.01.059

    • NLM

      Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059

    • Vancouver

      Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059

  • 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

    Source: Proceedings. Conference titles: World Chemistry Congress. Unidade: FCF

    Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/

  • Artigo de periodico

    Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition (2017)

    Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, COBRE

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      SOUZA, Frederico Bernardes de et al. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, v. 58, n. 11, p. 1057-1060, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.107. Acesso em: 28 jun. 2024.

    • APA

      Souza, F. B. de, Vasconcelos, S. N. S., Reis, J. S. dos, Pimenta, D. C., & Stefani, H. A. (2017). Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, 58( 11), 1057-1060. doi:10.1016/j.tetlet.2017.01.107

    • NLM

      Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107

    • Vancouver

      Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107

  • 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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    • 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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1039/c7nj01803g

  • Artigo de periodico

    Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles (2016)

    Souza, Frederico B; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Subjects: TECNOLOGIA DE MICRO-ONDAS, ALDEÍDOS

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    • ABNT

      SOUZA, Frederico B e PIMENTA, Daniel Carvalho e STEFANI, Hélio Alexandre. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, v. 57, n. 14, p. 1592-1596, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.02.105. Acesso em: 28 jun. 2024.

    • APA

      Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2016). Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, 57( 14), 1592-1596. doi:10.1016/j.tetlet.2016.02.105

    • NLM

      Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105

    • Vancouver

      Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105

  • 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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052

  • Artigo de periodico

    Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones (2015)

    Ali, Bakhat; Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre

    Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      ALI, Bakhat et al. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, v. 56, n. 28, p. 4234-4241, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.05.066. Acesso em: 28 jun. 2024.

    • APA

      Ali, B., Shamim, A., Vasconcelos, S. N. S., & Stefani, H. A. (2015). Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, 56( 28), 4234-4241. doi:10.1016/j.tetlet.2015.05.066

    • NLM

      Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066

    • Vancouver

      Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066

  • 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: 28 jun. 2024.

    • APA

      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. 28 ] 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. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059

  • Artigo de periodico

    Synthesis of functionalized N-triazolyl maleimides (2014)

    Stefani, Hélio Alexandre ; Ferreira, Fernando P; Ali, Bakhat; Pimenta, Daniel Carvalho

    Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, v. 55, n. 31, p. 4355-4358, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.05.095. Acesso em: 28 jun. 2024.

    • APA

      Stefani, H. A., Ferreira, F. P., Ali, B., & Pimenta, D. C. (2014). Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, 55( 31), 4355-4358. doi:10.1016/j.tetlet.2014.05.095

    • NLM

      Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095

    • Vancouver

      Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095

  • 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

    Source: Tetrahedron. Unidade: FCF

    Subjects: ITÉRBIO, SÍNTESE ORGÂNICA

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    • 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1016/j.tet.2013.11.107

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