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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: 05 jun. 2024.
    • APA

      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. 05 ] 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. 05 ] 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: 05 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. 05 ]
    • 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. 05 ]
  • 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: 05 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. 05 ] 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. 05 ] 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: 05 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. 05 ] 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. 05 ] 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: 05 jun. 2024.
    • APA

      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. 05 ] 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. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
  • Source: Drug Development and Industrial Pharmacy. Unidade: FCF

    Subjects: COSMETOLOGIA, UREIA, FLAVONÓIDES

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      BABY, André Rolim et al. Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design. Drug Development and Industrial Pharmacy, v. 35, n. 3, p. 272-282, 2009Tradução . . Disponível em: http://pdfserve.informaworld.com/276727_731408342_903083640.pdf. Acesso em: 05 jun. 2024.
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      Baby, A. R., Haroutiounian Filho, C. A., Sarruf, F. D., Pinto, C. A. S. de O., Kaneko, T. M., & Velasco, M. V. R. (2009). Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design. Drug Development and Industrial Pharmacy, 35( 3), 272-282. Recuperado de http://pdfserve.informaworld.com/276727_731408342_903083640.pdf
    • NLM

      Baby AR, Haroutiounian Filho CA, Sarruf FD, Pinto CAS de O, Kaneko TM, Velasco MVR. Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design [Internet]. Drug Development and Industrial Pharmacy. 2009 ; 35( 3): 272-282.[citado 2024 jun. 05 ] Available from: http://pdfserve.informaworld.com/276727_731408342_903083640.pdf
    • Vancouver

      Baby AR, Haroutiounian Filho CA, Sarruf FD, Pinto CAS de O, Kaneko TM, Velasco MVR. Influence of urea, isopropanol, and propylene glycol on rutin in vitro release from cosmetic semisolid systems estimated by factorial design [Internet]. Drug Development and Industrial Pharmacy. 2009 ; 35( 3): 272-282.[citado 2024 jun. 05 ] Available from: http://pdfserve.informaworld.com/276727_731408342_903083640.pdf
  • 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: 05 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
    • NLM

      Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 jun. 05 ] 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. 05 ] 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: 05 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. 05 ] 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. 05 ] 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: 05 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. 05 ] 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. 05 ] 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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      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: 05 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. 05 ] 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. 05 ] Available from: https://doi.org/10.1016/j.tet.2008.02.006
  • 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: 05 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. 05 ] 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. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
  • Source: Clinical Therapeutics. Unidade: FCF

    Subjects: BIOEQUIVALÊNCIA, ZIDOVUDINA (FARMACOCINÉTICA)

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      SERRA, Cristina Helena dos Reis et al. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study. Clinical Therapeutics, v. 30, n. 5, p. 902-908, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.clinthera.2008.05.003. Acesso em: 05 jun. 2024.
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      Serra, C. H. dos R., Koono, E. E. M., Kano, E. K., Schramm, S. G., Armando, Y. P., & Porta, V. (2008). Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study. Clinical Therapeutics, 30( 5), 902-908. doi:10.1016/j.clinthera.2008.05.003
    • NLM

      Serra CH dos R, Koono EEM, Kano EK, Schramm SG, Armando YP, Porta V. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study [Internet]. Clinical Therapeutics. 2008 ;30( 5): 902-908.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.clinthera.2008.05.003
    • Vancouver

      Serra CH dos R, Koono EEM, Kano EK, Schramm SG, Armando YP, Porta V. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study [Internet]. Clinical Therapeutics. 2008 ;30( 5): 902-908.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.clinthera.2008.05.003
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, POTÁSSIO, COBRE, SÍNTESE ORGÂNICA

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      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: 05 jun. 2024.
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      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. 05 ] 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. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: CARBOIDRATOS, ALDEÍDOS

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      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: 05 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. 05 ] 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. 05 ] 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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      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: 05 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. 05 ] 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. 05 ] 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: 05 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. 05 ] 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. 05 ] Available from: https://doi.org/10.1016/j.tet.2007.01.061
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ULTRASSONOGRAFIA, QUÍMICA FARMACÊUTICA

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    • ABNT

      GUZEN, Karla Pierdoná e CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings. Tetrahedron Letters, v. 47, n. 46, p. 8133-8136, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.09.043. Acesso em: 05 jun. 2024.
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      Guzen, K. P., Cella, R., & Stefani, H. A. (2006). Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings. Tetrahedron Letters, 47( 46), 8133-8136. doi:10.1016/j.tetlet.2006.09.043
    • NLM

      Guzen KP, Cella R, Stefani HA. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings [Internet]. Tetrahedron Letters. 2006 ; 47( 46): 8133-8136.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2006.09.043
    • Vancouver

      Guzen KP, Cella R, Stefani HA. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings [Internet]. Tetrahedron Letters. 2006 ; 47( 46): 8133-8136.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2006.09.043
  • Source: Tetrahedron. Unidade: FCF

    Subjects: ULTRASSONOGRAFIA, TELÚRIO, POTÁSSIO

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    • ABNT

      CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts. Tetrahedron, v. 62, n. 24, p. 5656-5662, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.03.090. Acesso em: 05 jun. 2024.
    • APA

      Cella, R., & Stefani, H. A. (2006). Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts. Tetrahedron, 62( 24), 5656-5662. doi:10.1016/j.tet.2006.03.090
    • NLM

      Cella R, Stefani HA. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts [Internet]. Tetrahedron. 2006 ; 62( 24): 5656-5662.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tet.2006.03.090
    • Vancouver

      Cella R, Stefani HA. Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts [Internet]. Tetrahedron. 2006 ; 62( 24): 5656-5662.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tet.2006.03.090
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: POTÁSSIO, TELÚRIO, QUÍMICA FARMACÊUTICA

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    • ABNT

      STEFANI, Hélio Alexandre et al. Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts. Tetrahedron Letters, v. 46, n. 4, p. 563-567, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2004.11.160. Acesso em: 05 jun. 2024.
    • APA

      Stefani, H. A., Cella, R., Dörr, F. A., Pereira, C. M. P. de, Zeni, G., & Gomes Junior, M. (2005). Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts. Tetrahedron Letters, 46( 4), 563-567. doi:10.1016/j.tetlet.2004.11.160
    • NLM

      Stefani HA, Cella R, Dörr FA, Pereira CMP de, Zeni G, Gomes Junior M. Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts [Internet]. Tetrahedron Letters. 2005 ; 46( 4): 563-567.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2004.11.160
    • Vancouver

      Stefani HA, Cella R, Dörr FA, Pereira CMP de, Zeni G, Gomes Junior M. Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts [Internet]. Tetrahedron Letters. 2005 ; 46( 4): 563-567.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2004.11.160
  • Source: Tetrahedron. Unidades: IQ, FCF

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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    • ABNT

      PETRAGNANI, Nicola e STEFANI, Hélio Alexandre. Advances in organic tellurium chemistry. Tetrahedron, v. 61, n. 7, p. 1613-1679, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2004.11.076. Acesso em: 05 jun. 2024.
    • APA

      Petragnani, N., & Stefani, H. A. (2005). Advances in organic tellurium chemistry. Tetrahedron, 61( 7), 1613-1679. doi:10.1016/j.tet.2004.11.076
    • NLM

      Petragnani N, Stefani HA. Advances in organic tellurium chemistry [Internet]. Tetrahedron. 2005 ; 61( 7): 1613-1679.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tet.2004.11.076
    • Vancouver

      Petragnani N, Stefani HA. Advances in organic tellurium chemistry [Internet]. Tetrahedron. 2005 ; 61( 7): 1613-1679.[citado 2024 jun. 05 ] Available from: https://doi.org/10.1016/j.tet.2004.11.076

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