Filtros : "Tetrahedron Letters" "2015" Limpar

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  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: ALCALOIDES, PALÁDIO, CATALISADORES, PRODUTOS NATURAIS

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    • ABNT

      FUMAGALLI, Fernando e EMERY, Flavio da Silva. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine. Tetrahedron Letters, v. 56, n. 18, p. 2307-2310, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.03.039. Acesso em: 10 nov. 2024.
    • APA

      Fumagalli, F., & Emery, F. da S. (2015). Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine. Tetrahedron Letters, 56( 18), 2307-2310. doi:10.1016/j.tetlet.2015.03.039
    • NLM

      Fumagalli F, Emery F da S. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine [Internet]. Tetrahedron Letters. 2015 ; 56( 18): 2307-2310.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.03.039
    • Vancouver

      Fumagalli F, Emery F da S. Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine [Internet]. Tetrahedron Letters. 2015 ; 56( 18): 2307-2310.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.03.039
  • 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
  • Source: Tetrahedron Letters. Unidade: FCFRP

    Subjects: CUCURBITALES, GLICOSÍDEOS, BIOLOGIA CELULAR

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    • ABNT

      MOROTTI, Ana L. M. et al. Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B. Tetrahedron Letters, v. 56, n. 2, p. 303-307, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.11.049. Acesso em: 10 nov. 2024.
    • APA

      Morotti, A. L. M., Lang, K. L., Carvalho, I., Schenkel, E. P., & Bernardes, L. S. C. (2015). Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B. Tetrahedron Letters, 56( 2), 303-307. doi:10.1016/j.tetlet.2014.11.049
    • NLM

      Morotti ALM, Lang KL, Carvalho I, Schenkel EP, Bernardes LSC. Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B [Internet]. Tetrahedron Letters. 2015 ; 56( 2): 303-307.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.11.049
    • Vancouver

      Morotti ALM, Lang KL, Carvalho I, Schenkel EP, Bernardes LSC. Semi-synthesis of new glycosidic triazole derivates of dihydrocucurbitacin B [Internet]. Tetrahedron Letters. 2015 ; 56( 2): 303-307.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2014.11.049
  • 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      BARBOSA, Jader da Silva e SILVA, Gil Valdo José da e CONSTANTINO, Maurício Gomes. One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction. Tetrahedron Letters, v. 56, n. 32, p. 4649-4652, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.06.061. Acesso em: 10 nov. 2024.
    • APA

      Barbosa, J. da S., Silva, G. V. J. da, & Constantino, M. G. (2015). One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction. Tetrahedron Letters, 56( 32), 4649-4652. doi:10.1016/j.tetlet.2015.06.061
    • NLM

      Barbosa J da S, Silva GVJ da, Constantino MG. One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction [Internet]. Tetrahedron Letters. 2015 ; 56( 32): 4649-4652.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.06.061
    • Vancouver

      Barbosa J da S, Silva GVJ da, Constantino MG. One-step synthesis of indanones through NbCl5-induced Friedel-Crafts reaction [Internet]. Tetrahedron Letters. 2015 ; 56( 32): 4649-4652.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.06.061
  • Source: Tetrahedron Letters. Unidade: IQSC

    Assunto: FÍSICO-QUÍMICA

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      ARAUJO, Yara Jaqueline Kerber et al. Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol. Tetrahedron Letters, v. 56, n. 13, p. 1696-1698, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.02.046. Acesso em: 10 nov. 2024.
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      Araujo, Y. J. K., Avvari, N. P., Paiva, D. R., Lima, D. P. de, & Beatriz, A. (2015). Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol. Tetrahedron Letters, 56( 13), 1696-1698. doi:10.1016/j.tetlet.2015.02.046
    • NLM

      Araujo YJK, Avvari NP, Paiva DR, Lima DP de, Beatriz A. Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol [Internet]. Tetrahedron Letters. 2015 ; 56( 13): 1696-1698.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.02.046
    • Vancouver

      Araujo YJK, Avvari NP, Paiva DR, Lima DP de, Beatriz A. Synthesis and enzymatic resolution of racemic 2,3-epoxy propyl esters obtained from glycerol [Internet]. Tetrahedron Letters. 2015 ; 56( 13): 1696-1698.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2015.02.046

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