Filtros : "Indexado no Research Alert" "FCF-FBF" Removidos: "Irã" "DAGLI, MARIA LUCIA ZAIDAN" Limpar

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  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SINGH, Fateh Veer e AMARAL, Mônica F. Z. J. e STEFANI, Hélio Alexandre. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, v. 50, n. 22, p. 2636-2639, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.078. Acesso em: 06 nov. 2024.
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      Singh, F. V., Amaral, M. F. Z. J., & Stefani, H. A. (2009). Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, 50( 22), 2636-2639. doi:10.1016/j.tetlet.2009.03.078
    • NLM

      Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
    • Vancouver

      Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
  • Source: Tetrahedron Letters. Unidades: FCF, IQ

    Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO

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      STEFANI, Hélio Alexandre et al. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, v. 50, n. 40, p. 5589-5595, 2009Tradução . . Acesso em: 06 nov. 2024.
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      Stefani, H. A., Pena, J. M., Gueogjian, K., Petragnani, N., Vaz, B. G., & Eberlin, M. N. (2009). Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, 50( 40), 5589-5595.
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      Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 nov. 06 ]
    • Vancouver

      Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 nov. 06 ]
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, POTÁSSIO, PALÁDIO

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      WEBER, Minéia et al. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, v. 50, n. 30, p. 4324-4327, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.04.127. Acesso em: 06 nov. 2024.
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      Weber, M., Singh, F. V., Vieira, A. S., Stefani, H. A., & Paixão, M. W. (2009). Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, 50( 30), 4324-4327. doi:10.1016/j.tetlet.2009.04.127
    • NLM

      Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
    • Vancouver

      Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: NUCLEOSÍDEOS, SELÊNIO (SÍNTESE), TELÚRIO (SÍNTESE)

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      BRAGA, Antonio Luiz et al. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, v. 50, n. 25, p. 3005-3007, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.164. Acesso em: 06 nov. 2024.
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      Braga, A. L., Severo Filho, W. A., Schwab, R. S., Rodrigues, O. E. D., Dornelles, L., Braga, H. C., & Lüdtke, D. (2009). Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, 50( 25), 3005-3007. doi:10.1016/j.tetlet.2009.03.164
    • NLM

      Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
    • Vancouver

      Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SINGH, Fateh Veer et al. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, v. 50, n. 20, p. 2312-2316, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.164. Acesso em: 06 nov. 2024.
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      Singh, F. V., Milagre, H. M. S., Eberlin, M. N., & Stefani, H. A. (2009). Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, 50( 20), 2312-2316. doi:10.1016/j.tetlet.2009.02.164
    • NLM

      Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
    • Vancouver

      Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
  • Source: Bioorganic and Medicinal Chemistry. Unidade: FCF

    Subjects: MODELAGEM MOLECULAR, STAPHYLOCOCCUS

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      JORGE, Salomão Dória et al. Design, synthesis, antimicrobial activity and molecular modeling studies of novel benzofuroxan derivatives against Staphylococcus aureus. Bioorganic and Medicinal Chemistry, v. 17, n. 8, p. 3028-3036, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2009.03.011. Acesso em: 06 nov. 2024.
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      Jorge, S. D., Masunari, A., Rangel-Yagui, C. de O., Pasqualoto, K. F. M., & Tavares, L. C. (2009). Design, synthesis, antimicrobial activity and molecular modeling studies of novel benzofuroxan derivatives against Staphylococcus aureus. Bioorganic and Medicinal Chemistry, 17( 8), 3028-3036. doi:10.1016/j.bmc.2009.03.011
    • NLM

      Jorge SD, Masunari A, Rangel-Yagui C de O, Pasqualoto KFM, Tavares LC. Design, synthesis, antimicrobial activity and molecular modeling studies of novel benzofuroxan derivatives against Staphylococcus aureus [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 8): 3028-3036.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.bmc.2009.03.011
    • Vancouver

      Jorge SD, Masunari A, Rangel-Yagui C de O, Pasqualoto KFM, Tavares LC. Design, synthesis, antimicrobial activity and molecular modeling studies of novel benzofuroxan derivatives against Staphylococcus aureus [Internet]. Bioorganic and Medicinal Chemistry. 2009 ; 17( 8): 3028-3036.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.bmc.2009.03.011
  • Source: Journal of Molecular Graphics and Modelling. Unidades: IFSC, FCF

    Subjects: TRYPANOSOMA CRUZI, CRISTALOGRAFIA, MODELAGEM MOLECULAR, PLANEJAMENTO DE FÁRMACOS, DOENÇA DE CHAGAS, ANTIPARASITÁRIOS, INIBIÇÃO

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      TROSSINI, Gustavo Henrique Goulart et al. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies. Journal of Molecular Graphics and Modelling, v. 28, n. 1, p. 3-11, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jmgm.2009.03.001. Acesso em: 06 nov. 2024.
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      Trossini, G. H. G., Guido, R. V. C., Oliva, G., Ferreira, E. I., & Andricopulo, A. D. (2009). Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies. Journal of Molecular Graphics and Modelling, 28( 1), 3-11. doi:10.1016/j.jmgm.2009.03.001
    • NLM

      Trossini GHG, Guido RVC, Oliva G, Ferreira EI, Andricopulo AD. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies [Internet]. Journal of Molecular Graphics and Modelling. 2009 ; 28( 1): 3-11.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jmgm.2009.03.001
    • Vancouver

      Trossini GHG, Guido RVC, Oliva G, Ferreira EI, Andricopulo AD. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies [Internet]. Journal of Molecular Graphics and Modelling. 2009 ; 28( 1): 3-11.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jmgm.2009.03.001
  • Source: JEADV - Journal of the European Academy of Dermatology and Venereology. Unidade: FCF

    Subjects: CABELO, EMULSÕES COSMÉTICAS

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      VICENTE, R. A. et al. Double-blind, randomized, placebo-controlled trial of a cream containing the Stryphnodendron adstringens (Martius) Coville bark extract for suppressing terminal hair growth. JEADV - Journal of the European Academy of Dermatology and Venereology, v. 23, n. 4, p. 410-414, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1468-3083.2009.03088.x. Acesso em: 06 nov. 2024.
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      Vicente, R. A., Leite e Silva, V. R., Baby, A. R., Velasco, M. V. R., & Bedin, A. (2009). Double-blind, randomized, placebo-controlled trial of a cream containing the Stryphnodendron adstringens (Martius) Coville bark extract for suppressing terminal hair growth. JEADV - Journal of the European Academy of Dermatology and Venereology, 23( 4), 410-414. doi:10.1111/j.1468-3083.2009.03088.x
    • NLM

      Vicente RA, Leite e Silva VR, Baby AR, Velasco MVR, Bedin A. Double-blind, randomized, placebo-controlled trial of a cream containing the Stryphnodendron adstringens (Martius) Coville bark extract for suppressing terminal hair growth [Internet]. JEADV - Journal of the European Academy of Dermatology and Venereology. 2009 ; 23( 4): 410-414.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1111/j.1468-3083.2009.03088.x
    • Vancouver

      Vicente RA, Leite e Silva VR, Baby AR, Velasco MVR, Bedin A. Double-blind, randomized, placebo-controlled trial of a cream containing the Stryphnodendron adstringens (Martius) Coville bark extract for suppressing terminal hair growth [Internet]. JEADV - Journal of the European Academy of Dermatology and Venereology. 2009 ; 23( 4): 410-414.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1111/j.1468-3083.2009.03088.x
  • Source: Tetrahedron. Unidade: FCF

    Subjects: ULTRASSONOGRAFIA, SÍNTESE ORGÂNICA

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      CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound in heterocycles chemistry. Tetrahedron, v. 65, n. 13, p. 2619-2641, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.12.027. Acesso em: 06 nov. 2024.
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      Cella, R., & Stefani, H. A. (2009). Ultrasound in heterocycles chemistry. Tetrahedron, 65( 13), 2619-2641. doi:10.1016/j.tet.2008.12.027
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      Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
    • Vancouver

      Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: BIODISPONIBILIDADE, FÁRMACOS, OLIGOSSACARÍDEOS

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      ASBAHR, Ana Carolina C. et al. Binary and ternary inclusion complexes of finasteride in HP 'beta' CD and polymers: preparation and characterization. Bioorganic & Medicinal Chemistry, v. 17, n. 7, p. 2718-2723, 2009Tradução . . Acesso em: 06 nov. 2024.
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      Asbahr, A. C. C., Franco, L., Barison, A., Silva, C. W. P., Ferraz, H. G., & Rodrigues, L. N. C. (2009). Binary and ternary inclusion complexes of finasteride in HP 'beta' CD and polymers: preparation and characterization. Bioorganic & Medicinal Chemistry, 17( 7), 2718-2723.
    • NLM

      Asbahr ACC, Franco L, Barison A, Silva CWP, Ferraz HG, Rodrigues LNC. Binary and ternary inclusion complexes of finasteride in HP 'beta' CD and polymers: preparation and characterization. Bioorganic & Medicinal Chemistry. 2009 ; 17( 7): 2718-2723.[citado 2024 nov. 06 ]
    • Vancouver

      Asbahr ACC, Franco L, Barison A, Silva CWP, Ferraz HG, Rodrigues LNC. Binary and ternary inclusion complexes of finasteride in HP 'beta' CD and polymers: preparation and characterization. Bioorganic & Medicinal Chemistry. 2009 ; 17( 7): 2718-2723.[citado 2024 nov. 06 ]
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: PLASMA, BIOEQUIVALÊNCIA, FARMACOCINÉTICA

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      PORTA, Valentina et al. HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies. Journal of Pharmaceutical and Biomedical Analysis, v. 46, n. 1, p. 143-147, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2007.10.007. Acesso em: 06 nov. 2024.
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      Porta, V., Schramm, S. G., Kano, E. K., Koono, E. E. M., Armando, Y. P., Fukuda, K., & Serra, C. H. dos R. (2008). HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies. Journal of Pharmaceutical and Biomedical Analysis, 46( 1), 143-147. doi:10.1016/j.jpba.2007.10.007
    • NLM

      Porta V, Schramm SG, Kano EK, Koono EEM, Armando YP, Fukuda K, Serra CH dos R. HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;46( 1): 143-147.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jpba.2007.10.007
    • Vancouver

      Porta V, Schramm SG, Kano EK, Koono EEM, Armando YP, Fukuda K, Serra CH dos R. HPLC-UV determination of metformin in human plasma for application in pharmacokinetics and bioequivalence studies [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;46( 1): 143-147.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jpba.2007.10.007
  • Source: Chemical Biology & Drug Design. Unidade: FCF

    Assunto: TUBERCULOSE (TRATAMENTO)

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      SILVA, Márcia da et al. Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design, v. 71, n. 2, p. 167-172, 2008Tradução . . Acesso em: 06 nov. 2024.
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      Silva, M. da, Menezes, C. M. de S., Ferreira, E. I., Leite, C. Q. F., Sato, D. N., Correia, C. C., et al. (2008). Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design, 71( 2), 167-172.
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      Silva M da, Menezes CM de S, Ferreira EI, Leite CQF, Sato DN, Correia CC, Pimenta CP, Botelho KCA. Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design. 2008 ;71( 2): 167-172.[citado 2024 nov. 06 ]
    • Vancouver

      Silva M da, Menezes CM de S, Ferreira EI, Leite CQF, Sato DN, Correia CC, Pimenta CP, Botelho KCA. Topliss method in the optimization of salicylic acid derivatives as potential antimycobacterial agents. Chemical Biology & Drug Design. 2008 ;71( 2): 167-172.[citado 2024 nov. 06 ]
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: FCF

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, DOENÇA DE CHAGAS

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      GRILLO, Renato et al. Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin. Journal of Pharmaceutical and Biomedical Analysis, v. 47, n. 2, p. 295-302, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2008.01.010. Acesso em: 06 nov. 2024.
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      Grillo, R., Melo, N. F. S. de, Moraes, C. M., Lima, R. de, Menezes, C. M. de S., Ferreira, E. I., et al. (2008). Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin. Journal of Pharmaceutical and Biomedical Analysis, 47( 2), 295-302. doi:10.1016/j.jpba.2008.01.010
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      Grillo R, Melo NFS de, Moraes CM, Lima R de, Menezes CM de S, Ferreira EI, Rosa AH, Fraceto LF. Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;47( 2): 295-302.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jpba.2008.01.010
    • Vancouver

      Grillo R, Melo NFS de, Moraes CM, Lima R de, Menezes CM de S, Ferreira EI, Rosa AH, Fraceto LF. Study of the interaction between hydroxymethylnitrofurazone and 2-hydroxypropyl-'beta'-cyclodextrin [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2008 ;47( 2): 295-302.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jpba.2008.01.010
  • Source: Synlett. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, PALÁDIO

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      SINGH, Fateh Veer e STEFANI, Hélio Alexandre. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides. Synlett, n. 20, p. 3221-3225, 2008Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf. Acesso em: 06 nov. 2024.
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      Singh, F. V., & Stefani, H. A. (2008). Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides. Synlett, ( 20), 3221-3225. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
    • NLM

      Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides [Internet]. Synlett. 2008 ;( 20): 3221-3225.[citado 2024 nov. 06 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
    • Vancouver

      Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed homocoupling of aryl n-butyl tellurides [Internet]. Synlett. 2008 ;( 20): 3221-3225.[citado 2024 nov. 06 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087244.pdf
  • Source: Journal of Chromatography A. Unidades: IQ, FCF

    Subjects: ELETROFORESE CAPILAR DE ZONA (MÉTODOS), ANTIFÚNGICOS

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      GALDOS, Angel Arturo Gaona et al. Development and validation of a method for quantitative determination of econazole nitrate in cream formulation by capillary zone electrophoresis. Journal of Chromatography A, v. 1092, n. 2, p. 301-305, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.chroma.2008.03.070. Acesso em: 06 nov. 2024.
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      Galdos, A. A. G., Zanolli Filho, L. A., Tavares, M. F. M., Aurora-Prado, M. S., Santoro, M. I. R. M., & Kedor-Hackmann, E. R. M. (2008). Development and validation of a method for quantitative determination of econazole nitrate in cream formulation by capillary zone electrophoresis. Journal of Chromatography A, 1092( 2), 301-305. doi:10.1016/j.chroma.2008.03.070
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      Galdos AAG, Zanolli Filho LA, Tavares MFM, Aurora-Prado MS, Santoro MIRM, Kedor-Hackmann ERM. Development and validation of a method for quantitative determination of econazole nitrate in cream formulation by capillary zone electrophoresis [Internet]. Journal of Chromatography A. 2008 ; 1092( 2): 301-305.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.chroma.2008.03.070
    • Vancouver

      Galdos AAG, Zanolli Filho LA, Tavares MFM, Aurora-Prado MS, Santoro MIRM, Kedor-Hackmann ERM. Development and validation of a method for quantitative determination of econazole nitrate in cream formulation by capillary zone electrophoresis [Internet]. Journal of Chromatography A. 2008 ; 1092( 2): 301-305.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.chroma.2008.03.070
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, TELÚRIO, REAÇÕES ORGÂNICAS

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      GUADAGNIN, Rafael Carlos et al. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, v. 49, n. 32, p. 4713-4716, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.05.129. Acesso em: 06 nov. 2024.
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      Guadagnin, R. C., Suganuma, C. A., Singh, F. V., Vieira, A. S., Cella, R., & Stefani, H. A. (2008). Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts. Tetrahedron Letters, 49( 32), 4713-4716. doi:10.1016/j.tetlet.2008.05.129
    • NLM

      Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
    • Vancouver

      Guadagnin RC, Suganuma CA, Singh FV, Vieira AS, Cella R, Stefani HA. Chemoselective cross-coupling Suzuki-Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts [Internet]. Tetrahedron Letters. 2008 ; 49( 32): 4713-4716.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
  • Source: Bioorganic and Medicinal Chemistry. Unidade: FCF

    Subjects: LEISHMANIA, FARMACOLOGIA, ANTIPROTOZOÁRIOS

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    • ABNT

      RANDO, Daniela Gonçales et al. Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides. Bioorganic and Medicinal Chemistry, v. 16, n. 14, p. 6724-6731, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2008.05.076. Acesso em: 06 nov. 2024.
    • APA

      Rando, D. G., Avery, M. A., Tekwani, B. L., Khan, S. I., & Ferreira, E. I. (2008). Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides. Bioorganic and Medicinal Chemistry, 16( 14), 6724-6731. doi:10.1016/j.bmc.2008.05.076
    • NLM

      Rando DG, Avery MA, Tekwani BL, Khan SI, Ferreira EI. Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides [Internet]. Bioorganic and Medicinal Chemistry. 2008 ; 16( 14): 6724-6731.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.bmc.2008.05.076
    • Vancouver

      Rando DG, Avery MA, Tekwani BL, Khan SI, Ferreira EI. Antileishmanial activity screening of 5-nitro-2-heterocyclic benzylidene hydrazides [Internet]. Bioorganic and Medicinal Chemistry. 2008 ; 16( 14): 6724-6731.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.bmc.2008.05.076
  • Source: Journal of Organometallic Chemistry. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, BORO

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    • ABNT

      BELLOMO, Ana e GONZALES, David e STEFANI, Hélio Alexandre. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach. Journal of Organometallic Chemistry, v. 693, n. 6, p. 1136-1142, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.01.006. Acesso em: 06 nov. 2024.
    • APA

      Bellomo, A., Gonzales, D., & Stefani, H. A. (2008). Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach. Journal of Organometallic Chemistry, 693( 6), 1136-1142. doi:10.1016/j.jorganchem.2008.01.006
    • NLM

      Bellomo A, Gonzales D, Stefani HA. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach [Internet]. Journal of Organometallic Chemistry. 2008 ;693( 6): 1136-1142.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.01.006
    • Vancouver

      Bellomo A, Gonzales D, Stefani HA. Synthesis of unnatural cyclitols via a combined enzymatic-palladium catalysis approach [Internet]. Journal of Organometallic Chemistry. 2008 ;693( 6): 1136-1142.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.01.006
  • Source: Tetrahedron. Unidade: FCF

    Subjects: POTÁSSIO (SÍNTESE), SÍNTESE ORGÂNICA

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      VIEIRA, Adriano Siqueira et al. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions. Tetrahedron, v. 64, n. 30-31, p. 7234-7241, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.05.085. Acesso em: 06 nov. 2024.
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      Vieira, A. S., Fiorante, P. de F., Zukerman-Schpector, J., Alves, D., Botteselle, G. D. V., & Stefani, H. A. (2008). Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions. Tetrahedron, 64( 30-31), 7234-7241. doi:10.1016/j.tet.2008.05.085
    • NLM

      Vieira AS, Fiorante P de F, Zukerman-Schpector J, Alves D, Botteselle GDV, Stefani HA. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions [Internet]. Tetrahedron. 2008 ; 64( 30-31): 7234-7241.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
    • Vancouver

      Vieira AS, Fiorante P de F, Zukerman-Schpector J, Alves D, Botteselle GDV, Stefani HA. Synthesis of potassium and tetra n-butylammonium 2-substituted-1,3- dithianotrifluoroborate salts and addition to chiral cyclic N-acyliminium ions [Internet]. Tetrahedron. 2008 ; 64( 30-31): 7234-7241.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
  • Source: Tetrahedron. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, SÍNTESE ORGÂNICA

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    • ABNT

      VIEIRA, Adriano Siqueira et al. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles. Tetrahedron, v. 64, n. 15, p. 3306-3314, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2008.02.006. Acesso em: 06 nov. 2024.
    • APA

      Vieira, A. S., Ferreira, F. da P., Fiorante, P. de F., Guadagnin, R. C., & Stefani, H. A. (2008). Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles. Tetrahedron, 64( 15), 3306-3314. doi:10.1016/j.tet.2008.02.006
    • NLM

      Vieira AS, Ferreira F da P, Fiorante P de F, Guadagnin RC, Stefani HA. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles [Internet]. Tetrahedron. 2008 ;64( 15): 3306-3314.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
    • Vancouver

      Vieira AS, Ferreira F da P, Fiorante P de F, Guadagnin RC, Stefani HA. Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles [Internet]. Tetrahedron. 2008 ;64( 15): 3306-3314.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006

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