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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 jun. 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 jun. 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 jun. 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 jun. 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.
    • NLM

      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 jun. 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 jun. 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 jun. 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 jun. 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 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
  • Source: Journal of AOAC International. Unidade: FCF

    Subjects: MEDICAMENTO, FÁRMACOS, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA

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      SOARES, Renata et al. Determination of atropine enantiomers in ophthalmic solutions by liquid chromatography using a chiral AGP`registred mark´ column. Journal of AOAC International, v. 92, n. 6, p. 1663-1672, 2009Tradução . . Disponível em: http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.92.6.1663. Acesso em: 06 jun. 2024.
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      Soares, R., Singh, A. K., Kedor-Hackmann, E. R. M., & Santoro, M. I. R. M. (2009). Determination of atropine enantiomers in ophthalmic solutions by liquid chromatography using a chiral AGP`registred mark´ column. Journal of AOAC International, 92( 6), 1663-1672. Recuperado de http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.92.6.1663
    • NLM

      Soares R, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Determination of atropine enantiomers in ophthalmic solutions by liquid chromatography using a chiral AGP`registred mark´ column [Internet]. Journal of AOAC International. 2009 ; 92( 6): 1663-1672.[citado 2024 jun. 06 ] Available from: http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.92.6.1663
    • Vancouver

      Soares R, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Determination of atropine enantiomers in ophthalmic solutions by liquid chromatography using a chiral AGP`registred mark´ column [Internet]. Journal of AOAC International. 2009 ; 92( 6): 1663-1672.[citado 2024 jun. 06 ] Available from: http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.92.6.1663
  • 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 jun. 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 jun. 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 jun. 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 jun. 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 jun. 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 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
  • Source: Chromatographia. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA, HIDRÓLISE

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      RIVAS-GRANIZO, Patricia Elizabeth e SANTOS, Silvia Regina Cavani Jorge e FERRAZ, Humberto Gomes. Development of a stability-indicating LC assay method for determination of chloroquine. Chromatographia, v. 69, p. S137-S141, 2009Tradução . . Acesso em: 06 jun. 2024.
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      Rivas-Granizo, P. E., Santos, S. R. C. J., & Ferraz, H. G. (2009). Development of a stability-indicating LC assay method for determination of chloroquine. Chromatographia, 69, S137-S141.
    • NLM

      Rivas-Granizo PE, Santos SRCJ, Ferraz HG. Development of a stability-indicating LC assay method for determination of chloroquine. Chromatographia. 2009 ; 69 S137-S141.[citado 2024 jun. 06 ]
    • Vancouver

      Rivas-Granizo PE, Santos SRCJ, Ferraz HG. Development of a stability-indicating LC assay method for determination of chloroquine. Chromatographia. 2009 ; 69 S137-S141.[citado 2024 jun. 06 ]
  • Source: Chromatographia. Unidade: FCF

    Subjects: CROMATOGRAFIA LÍQUIDA, EXTRAÇÃO DE LÍQUIDOS, ZIDOVUDINA

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      SOUZA, Jacqueline de et al. LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia, v. 69, p. S231-S235, 2009Tradução . . Acesso em: 06 jun. 2024.
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      Souza, J. de, Kano, E. K., Koono, E. E. M., Schramm, S. G., Porta, V., & Storpirtis, S. (2009). LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia, 69, S231-S235.
    • NLM

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia. 2009 ; 69 S231-S235.[citado 2024 jun. 06 ]
    • Vancouver

      Souza J de, Kano EK, Koono EEM, Schramm SG, Porta V, Storpirtis S. LC-UC methodology for simultaneous determination of lamivudine and zidovudine in plasma by liquid-liquid extraction. Chromatographia. 2009 ; 69 S231-S235.[citado 2024 jun. 06 ]
  • 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 jun. 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 jun. 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 jun. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
  • 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 jun. 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 jun. 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 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
  • 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 jun. 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 jun. 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 jun. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
  • Source: Journal of AOAC International. Unidade: FCF

    Subjects: ESPECTROMETRIA (MÉTODOS), CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA (MÉTODOS), FARMACOLOGIA

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      SINGH, Anil Kumar et al. Development and validation of sensitive methods for determination of sibutramine hydrochloride monohydrate and direct enantiomeric separation on a protein-based chiral stationary phase. Journal of AOAC International, v. 91, n. 3, p. 572-579, 2008Tradução . . Acesso em: 06 jun. 2024.
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      Singh, A. K., García, P. L., Gomes, F. P., Yano, H. M., Auricchio, M. T., Kedor-Hackmann, E. R. M., & Santoro, M. I. R. M. (2008). Development and validation of sensitive methods for determination of sibutramine hydrochloride monohydrate and direct enantiomeric separation on a protein-based chiral stationary phase. Journal of AOAC International, 91( 3), 572-579.
    • NLM

      Singh AK, García PL, Gomes FP, Yano HM, Auricchio MT, Kedor-Hackmann ERM, Santoro MIRM. Development and validation of sensitive methods for determination of sibutramine hydrochloride monohydrate and direct enantiomeric separation on a protein-based chiral stationary phase. Journal of AOAC International. 2008 ; 91( 3): 572-579.[citado 2024 jun. 06 ]
    • Vancouver

      Singh AK, García PL, Gomes FP, Yano HM, Auricchio MT, Kedor-Hackmann ERM, Santoro MIRM. Development and validation of sensitive methods for determination of sibutramine hydrochloride monohydrate and direct enantiomeric separation on a protein-based chiral stationary phase. Journal of AOAC International. 2008 ; 91( 3): 572-579.[citado 2024 jun. 06 ]
  • Source: Journal of AOAC International. Unidade: FCF

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, COSMÉTICOS (FORMULAÇÃO)

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      BATISTA, Ivani Aparecida Soares de Andrade et al. Quantitative determination of dimethylaminoethanol in cosmetic formulations by nuclear magnetic resonance spectroscopy. Journal of AOAC International, v. 91, n. 6, p. 1303-1308, 2008Tradução . . Disponível em: http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.91.6.1303. Acesso em: 06 jun. 2024.
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      Batista, I. A. S. de A., Gonçalves, M. I. de A., Singh, A. K., Kedor-Hackmann, E. R. M., & Santoro, M. I. R. M. (2008). Quantitative determination of dimethylaminoethanol in cosmetic formulations by nuclear magnetic resonance spectroscopy. Journal of AOAC International, 91( 6), 1303-1308. Recuperado de http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.91.6.1303
    • NLM

      Batista IAS de A, Gonçalves MI de A, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Quantitative determination of dimethylaminoethanol in cosmetic formulations by nuclear magnetic resonance spectroscopy [Internet]. Journal of AOAC International. 2008 ; 91( 6): 1303-1308.[citado 2024 jun. 06 ] Available from: http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.91.6.1303
    • Vancouver

      Batista IAS de A, Gonçalves MI de A, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Quantitative determination of dimethylaminoethanol in cosmetic formulations by nuclear magnetic resonance spectroscopy [Internet]. Journal of AOAC International. 2008 ; 91( 6): 1303-1308.[citado 2024 jun. 06 ] Available from: http://www.atypon-link.com/AOAC/doi/pdf/10.5555/jaoi.91.6.1303
  • Source: Tetrahedron. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, SÍNTESE ORGÂNICA

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      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 jun. 2024.
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      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 jun. 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 jun. 06 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
  • Source: Journal of Ethnopharmacology. Unidades: IQ, FCF

    Subjects: PLANTAS MEDICINAIS, METABÓLITOS SECUNDÁRIOS

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      ISHIKAWA, Tati et al. Evaluation of gastroprotective activity of Plinia edulis (Vell.) Sobral (Myrtaceae) leaves in rats. Journal of Ethnopharmacology, v. 118, n. 3, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jep.2008.05.007. Acesso em: 06 jun. 2024.
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      Ishikawa, T., Donatini, R. dos S., Diaz, I. E. C., Yoshida, M., Bacchi, E. M., & Kato, E. T. M. (2008). Evaluation of gastroprotective activity of Plinia edulis (Vell.) Sobral (Myrtaceae) leaves in rats. Journal of Ethnopharmacology, 118( 3). doi:10.1016/j.jep.2008.05.007
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      Ishikawa T, Donatini R dos S, Diaz IEC, Yoshida M, Bacchi EM, Kato ETM. Evaluation of gastroprotective activity of Plinia edulis (Vell.) Sobral (Myrtaceae) leaves in rats [Internet]. Journal of Ethnopharmacology. 2008 ; 118( 3):[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.jep.2008.05.007
    • Vancouver

      Ishikawa T, Donatini R dos S, Diaz IEC, Yoshida M, Bacchi EM, Kato ETM. Evaluation of gastroprotective activity of Plinia edulis (Vell.) Sobral (Myrtaceae) leaves in rats [Internet]. Journal of Ethnopharmacology. 2008 ; 118( 3):[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.jep.2008.05.007
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ALDEÍDOS, SÍNTESE ORGÂNICA, BORO

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      CELLA, Rodrigo e VENTUROSO, Raphael Costa e STEFANI, Hélio Alexandre. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes. Tetrahedron Letters, v. 49, n. 1, p. 16-19, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.031. Acesso em: 06 jun. 2024.
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      Cella, R., Venturoso, R. C., & Stefani, H. A. (2008). Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes. Tetrahedron Letters, 49( 1), 16-19. doi:10.1016/j.tetlet.2007.11.031
    • NLM

      Cella R, Venturoso RC, Stefani HA. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes [Internet]. Tetrahedron Letters. 2008 ;49( 1): 16-19.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
    • Vancouver

      Cella R, Venturoso RC, Stefani HA. Stereoselective synthesis of the dolastatin units by organotrifluoroborates additions to alpha-amino aldehydes [Internet]. Tetrahedron Letters. 2008 ;49( 1): 16-19.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, COBRE, SÍNTESE ORGÂNICA

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    • ABNT

      PAIXÃO, Márcio Weber et al. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes. Tetrahedron Letters, v. 49, n. 15, p. 2366-2370, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.02.083. Acesso em: 06 jun. 2024.
    • APA

      Paixão, M. W., Weber, M., Braga, A. L., Azeredo, J. B. de, Deobald, A. M., & Stefani, H. A. (2008). Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes. Tetrahedron Letters, 49( 15), 2366-2370. doi:10.1016/j.tetlet.2008.02.083
    • NLM

      Paixão MW, Weber M, Braga AL, Azeredo JB de, Deobald AM, Stefani HA. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2366-2370.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
    • Vancouver

      Paixão MW, Weber M, Braga AL, Azeredo JB de, Deobald AM, Stefani HA. Copper salt-catalyzed homo-coupling reaction of potassium alkynyltrifluoroborates: a simple and efficient synthesis of symmetrical 1,3-diynes [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2366-2370.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: CARBOIDRATOS, ALDEÍDOS

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    • ABNT

      APPELT, Helmoz Roseniaim et al. Carbohydrates in asymmetric synthesis: enantioselective allylation of aldehydes. Tetrahedron Letters, v. 49, n. 33, p. 4956-4957, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.05.109. Acesso em: 06 jun. 2024.
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      Appelt, H. R., Limberger, J. B., Weber, M., Rodrigues, O. E. D., Oliveira, J. S. de, Lüdtke, D., & Braga, A. L. (2008). Carbohydrates in asymmetric synthesis: enantioselective allylation of aldehydes. Tetrahedron Letters, 49( 33), 4956-4957. doi:10.1016/j.tetlet.2008.05.109
    • NLM

      Appelt HR, Limberger JB, Weber M, Rodrigues OED, Oliveira JS de, Lüdtke D, Braga AL. Carbohydrates in asymmetric synthesis: enantioselective allylation of aldehydes [Internet]. Tetrahedron Letters. 2008 ; 49( 33): 4956-4957.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.109
    • Vancouver

      Appelt HR, Limberger JB, Weber M, Rodrigues OED, Oliveira JS de, Lüdtke D, Braga AL. Carbohydrates in asymmetric synthesis: enantioselective allylation of aldehydes [Internet]. Tetrahedron Letters. 2008 ; 49( 33): 4956-4957.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.109
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: CATÁLISE, SÍNTESE ORGÂNICA

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    • ABNT

      SCHWAB, Ricardo S. et al. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide. Tetrahedron Letters, v. 49, n. 34, p. 5094-5097, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.06.031. Acesso em: 06 jun. 2024.
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      Schwab, R. S., Galetto, F. Z., Azeredo, J. B. de, Braga, A. L., Lüdtke, D. S., & Paixão, M. W. (2008). Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide. Tetrahedron Letters, 49( 34), 5094-5097. doi:10.1016/j.tetlet.2008.06.031
    • NLM

      Schwab RS, Galetto FZ, Azeredo JB de, Braga AL, Lüdtke DS, Paixão MW. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide [Internet]. Tetrahedron Letters. 2008 ; 49( 34): 5094-5097.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.06.031
    • Vancouver

      Schwab RS, Galetto FZ, Azeredo JB de, Braga AL, Lüdtke DS, Paixão MW. Organocatalytic asymmetric aldol reactions mediated by a cysteine-derived prolinamide [Internet]. Tetrahedron Letters. 2008 ; 49( 34): 5094-5097.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tetlet.2008.06.031
  • Source: Tetrahedron. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, BORO

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    • ABNT

      STEFANI, Hélio Alexandre e CELLA, Rodrigo e VIEIRA, Adriano Siqueira. Recent advances in organotrifluoroborates chemistry. Tetrahedron, v. 63, n. 18, p. 3623-3658, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.01.061. Acesso em: 06 jun. 2024.
    • APA

      Stefani, H. A., Cella, R., & Vieira, A. S. (2007). Recent advances in organotrifluoroborates chemistry. Tetrahedron, 63( 18), 3623-3658. doi:10.1016/j.tet.2007.01.061
    • NLM

      Stefani HA, Cella R, Vieira AS. Recent advances in organotrifluoroborates chemistry [Internet]. Tetrahedron. 2007 ; 63( 18): 3623-3658.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tet.2007.01.061
    • Vancouver

      Stefani HA, Cella R, Vieira AS. Recent advances in organotrifluoroborates chemistry [Internet]. Tetrahedron. 2007 ; 63( 18): 3623-3658.[citado 2024 jun. 06 ] Available from: https://doi.org/10.1016/j.tet.2007.01.061

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