Filtros : "FCF004" "Tetrahedron Letters" Removidos: "Estudos Avançados" "República Tcheca" "ENSINO CIÊNCIAS" Limpar

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  • 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: 29 set. 2024.
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      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: 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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
  • 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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: TECNOLOGIA DE MICRO-ONDAS, ALDEÍDOS

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      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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
  • 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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
  • 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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
  • 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.
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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 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: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: TELÚRIO, SÍNTESE ORGÂNICA

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      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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINOÁCIDOS, ITÉRBIO

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      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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.133
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      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: 29 set. 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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: POTÁSSIO, SÍNTESE ORGÂNICA

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      STEFANI, Hélio Alexandre et al. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, v. 52, n. 33, p. 4256-4261 + Supplementary Materials ( S1-S7), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.04.072. Acesso em: 29 set. 2024.
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      Stefani, H. A., Vieira, A. S., Amaral, M. F. Z. J., & Cooper, L. (2011). Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, 52( 33), 4256-4261 + Supplementary Materials ( S1-S7). doi:10.1016/j.tetlet.2011.04.072
    • NLM

      Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
    • Vancouver

      Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: AMINOÁCIDOS, SÍNTESE ORGÂNICA

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      STEFANI, Hélio Alexandre e AMARAL, Monica Franco Zanini Junqueira e JUARISTI, Eusebio. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, v. 52, n. 9, p. 1014-1019, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.12.087. Acesso em: 29 set. 2024.
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      Stefani, H. A., Amaral, M. F. Z. J., & Juaristi, E. (2011). Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, 52( 9), 1014-1019. doi:10.1016/j.tetlet.2010.12.087
    • NLM

      Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
    • Vancouver

      Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
  • Source: Tetrahedron Letters. Unidades: FCF, IQ

    Subjects: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS

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      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: 29 set. 2024.
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      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 set. 29 ] 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 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ULTRASSOM, SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      STEFANI, Hélio Alexandre e CANDUZINI, Hugo A e MANARIN, Flávia. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition. Tetrahedron Letters, v. 52, n. 46, p. 6086-6090 : + Supplementary materials ( S1-S10), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.09.004. Acesso em: 29 set. 2024.
    • APA

      Stefani, H. A., Canduzini, H. A., & Manarin, F. (2011). Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition. Tetrahedron Letters, 52( 46), 6086-6090 : + Supplementary materials ( S1-S10). doi:10.1016/j.tetlet.2011.09.004
    • NLM

      Stefani HA, Canduzini HA, Manarin F. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition [Internet]. Tetrahedron Letters. 2011 ; 52( 46): 6086-6090 : + Supplementary materials ( S1-S10).[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2011.09.004
    • Vancouver

      Stefani HA, Canduzini HA, Manarin F. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition [Internet]. Tetrahedron Letters. 2011 ; 52( 46): 6086-6090 : + Supplementary materials ( S1-S10).[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2011.09.004
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      GUZEN, Karla Pierdoná et al. Eco-friendly synthesis of imines by ultrasound irradiation. Tetrahedron Letters, v. 48, n. 10, p. 1845-1848, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.01.014. Acesso em: 29 set. 2024.
    • APA

      Guzen, K. P., Guarezemini, A. S., Órfão, A. T. G., Cella, R., Pereira, C. M. P. de, & Stefani, H. A. (2007). Eco-friendly synthesis of imines by ultrasound irradiation. Tetrahedron Letters, 48( 10), 1845-1848. doi:10.1016/j.tetlet.2007.01.014
    • NLM

      Guzen KP, Guarezemini AS, Órfão ATG, Cella R, Pereira CMP de, Stefani HA. Eco-friendly synthesis of imines by ultrasound irradiation [Internet]. Tetrahedron Letters. 2007 ; 48( 10): 1845-1848.[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2007.01.014
    • Vancouver

      Guzen KP, Guarezemini AS, Órfão ATG, Cella R, Pereira CMP de, Stefani HA. Eco-friendly synthesis of imines by ultrasound irradiation [Internet]. Tetrahedron Letters. 2007 ; 48( 10): 1845-1848.[citado 2024 set. 29 ] Available from: https://doi.org/10.1016/j.tetlet.2007.01.014

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