Filtros : "Schpector, Júlio Zukerman" Removido: "IQ" Limpar

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  • Source: Synthetic Communications. Unidade: FCF

    Subjects: COMPOSTOS HETEROCÍCLICOS, SÍNTESE QUÍMICA

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    • ABNT

      BALFOUR, Michael N et al. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, v. 49, n. 3, p. 351-358, 2019Tradução . . Disponível em: https://doi.org/10.1080/00397911.2018.1545032. Acesso em: 29 set. 2024.
    • APA

      Balfour, M. N., Schpector, J. Z., Rodriguez, M. J. D., Reis, J. S. dos, Esteves, C. H. A., & Stefani, H. A. (2019). Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, 49( 3), 351-358. doi:10.1080/00397911.2018.1545032
    • NLM

      Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 set. 29 ] Available from: https://doi.org/10.1080/00397911.2018.1545032
    • Vancouver

      Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 set. 29 ] Available from: https://doi.org/10.1080/00397911.2018.1545032
  • Source: Synthetic Communications. Unidade: FCF

    Subjects: PALÁDIO, COMPOSTOS HETEROCÍCLICOS

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    • ABNT

      REIS, Joel Savi dos et al. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, v. 49, n. 10, p. 1252-1261, 2019Tradução . . Disponível em: https://doi.org/10.1080/00397911.2019.1595657. Acesso em: 29 set. 2024.
    • APA

      Reis, J. S. dos, Caracelli, I., Schpector, J. Z., & Stefani, H. A. (2019). Sonogashira cross-coupling in iodo-containing 2-aryloxazolines. Synthetic Communications, 49( 10), 1252-1261. doi:10.1080/00397911.2019.1595657
    • NLM

      Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.[citado 2024 set. 29 ] Available from: https://doi.org/10.1080/00397911.2019.1595657
    • Vancouver

      Reis JS dos, Caracelli I, Schpector JZ, Stefani HA. Sonogashira cross-coupling in iodo-containing 2-aryloxazolines [Internet]. Synthetic Communications. 2019 ; 49( 10): 1252-1261.[citado 2024 set. 29 ] Available from: https://doi.org/10.1080/00397911.2019.1595657
  • Source: Advanced Synthesis and Catalysis. Unidade: FCF

    Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO

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      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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1002/adsc.201900142
  • 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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
  • Source: Arabian Journal of Chemistry. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS

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    • ABNT

      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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
  • 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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1515/zkri-2015-1911
  • 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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
  • Source: Zeitschrift fur Kristallographie. Unidade: FCF

    Subjects: DIFRAÇÃO POR RAIOS X, TELÚRIO

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      SCHPECTOR, Júlio Zukerman et al. Crystal and molecular structures of dichloro((Z)-2-chloro-2-phenylvinyl)(organo)tellurium(IV) for organo = n-butyl and phenyl. Zeitschrift fur Kristallographie, v. 223, n. 8, p. 536-541, 2008Tradução . . Disponível em: https://doi.org/10.1524/zkri.2008.0059. Acesso em: 29 set. 2024.
    • APA

      Schpector, J. Z., Stefani, H. A., Guadagnin, R. C., Suganuma, C. A., & Tiekink, E. R. T. (2008). Crystal and molecular structures of dichloro((Z)-2-chloro-2-phenylvinyl)(organo)tellurium(IV) for organo = n-butyl and phenyl. Zeitschrift fur Kristallographie, 223( 8), 536-541. doi:10.1524/zkri.2008.0059
    • NLM

      Schpector JZ, Stefani HA, Guadagnin RC, Suganuma CA, Tiekink ERT. Crystal and molecular structures of dichloro((Z)-2-chloro-2-phenylvinyl)(organo)tellurium(IV) for organo = n-butyl and phenyl [Internet]. Zeitschrift fur Kristallographie. 2008 ; 223( 8): 536-541.[citado 2024 set. 29 ] Available from: https://doi.org/10.1524/zkri.2008.0059
    • Vancouver

      Schpector JZ, Stefani HA, Guadagnin RC, Suganuma CA, Tiekink ERT. Crystal and molecular structures of dichloro((Z)-2-chloro-2-phenylvinyl)(organo)tellurium(IV) for organo = n-butyl and phenyl [Internet]. Zeitschrift fur Kristallographie. 2008 ; 223( 8): 536-541.[citado 2024 set. 29 ] Available from: https://doi.org/10.1524/zkri.2008.0059

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