Filtros : "Universidade Federal de São Carlos (UFSCar)" "STEFANI, HELIO ALEXANDRE" Limpar

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

    Subjects: ALDEÍDOS, ESTEREOQUÍMICA

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      VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 09 maio 2024.
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      Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Pimenta, D. C., & Stefani, H. A. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564
    • NLM

      Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2024 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1002/adsc.201900564
  • 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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1002/adsc.201900142
  • 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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1039/c8nj01543k
  • 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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
  • 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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1055/s-0036-1589090
  • Source: Molecular Diversity. Unidade: FCF

    Subjects: ALFA-AMINOÁCIDOS, SÍNTESE ORGÂNICA

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      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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1007/s11030-017-9764-5
  • Source: ChemistrySelect. Unidade: FCF

    Subjects: PALÁDIO, QUÍMICA FARMACÊUTICA

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      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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1002/slct.201701197
  • 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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
  • 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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1039/c7nj01803g
  • Source: Zeitschrift fur Kristallographie. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, CRISTALOGRAFIA ESTRUTURAL

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      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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1515/zkri-2015-1911
  • Source: ChemistrySelect. Unidades: IQ, FCF

    Subjects: MECANISMOS, FLUORESCÊNCIA

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      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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1002/slct.201601526
  • Source: Zeitschrift fur Kristallographie - Crystalline Materials. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, COMPOSTOS ORGÂNICOS

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      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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1515/zkri-2016-1931
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, PALÁDIO

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      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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINAS, CATÁLISE

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      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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
  • Source: Molecules. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, SÍNTESE ORGÂNICA

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      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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.3390/molecules19021990
  • Source: European Journal of Organic Chemistry. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, TELÚRIO

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      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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1002/ejoc.201300009
  • 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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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    • 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: 09 maio 2024.
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      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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
  • Source: European Journal of Medicinal Chemistry. Unidade: FCF

    Subjects: AMINOÁCIDOS, ANTI-INFLAMATÓRIOS

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    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives. European Journal of Medicinal Chemistry, v. 47, n. 1, p. 52-58 : + Supplementary materials ( S1-S6), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2011.10.018. Acesso em: 09 maio 2024.
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      Stefani, H. A., Botteselle, G. D. V., Zukerman-Schpector, J., Caracelli, I., Corrêa, D. da S., Farsky, S. H. P., et al. (2012). Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives. European Journal of Medicinal Chemistry, 47( 1), 52-58 : + Supplementary materials ( S1-S6). doi:10.1016/j.ejmech.2011.10.018
    • NLM

      Stefani HA, Botteselle GDV, Zukerman-Schpector J, Caracelli I, Corrêa D da S, Farsky SHP, Machado ID, Santin JR, Hebeda CB. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives [Internet]. European Journal of Medicinal Chemistry. 2012 ; 47( 1): 52-58 : + Supplementary materials ( S1-S6).[citado 2024 maio 09 ] Available from: https://doi.org/10.1016/j.ejmech.2011.10.018
    • Vancouver

      Stefani HA, Botteselle GDV, Zukerman-Schpector J, Caracelli I, Corrêa D da S, Farsky SHP, Machado ID, Santin JR, Hebeda CB. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives [Internet]. European Journal of Medicinal Chemistry. 2012 ; 47( 1): 52-58 : + Supplementary materials ( S1-S6).[citado 2024 maio 09 ] Available from: https://doi.org/10.1016/j.ejmech.2011.10.018
  • Source: European Journal of Medicinal Chemistry. Unidades: ICB, FCF

    Subjects: FISIOLOGIA, FARMACOLOGIA

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      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: 09 maio 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 maio 09 ] 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 maio 09 ] Available from: https://doi.org/10.1016/j.ejmech.2012.10.010

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