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  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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    • ABNT

      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: 12 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. 12 ] 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. 12 ] 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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    • ABNT

      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: 12 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.
    • 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 nov. 12 ]
    • 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. 12 ]
  • 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: 12 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. 12 ] 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. 12 ] 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: 12 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. 12 ] 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. 12 ] 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: 12 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. 12 ] 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. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
  • Source: Tetrahedron Asymmetry. Unidade: IQ

    Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA

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      ANDRADE, Leandro Helgueira e PIOVAN, Leandro e PASQUINI, Mônica D`Arcadia. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, v. 20, n. 13, p. 1521-1525, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.05.033. Acesso em: 12 nov. 2024.
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      Andrade, L. H., Piovan, L., & Pasquini, M. D. `A. (2009). Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, 20( 13), 1521-1525. doi:10.1016/j.tetasy.2009.05.033
    • NLM

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
    • Vancouver

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA

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      KEPPLER, Artur Franz et al. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, v. 50, n. 19, p. 2181-2184, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.158. Acesso em: 12 nov. 2024.
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      Keppler, A. F., Gariani, R. A., Lopes, D. G., & Comasseto, J. V. (2009). Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, 50( 19), 2181-2184. doi:10.1016/j.tetlet.2009.02.158
    • NLM

      Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
    • Vancouver

      Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: PALÁDIO, CANDIDA

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      ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira e PEDROZO, Eliane Correa. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, v. 50, n. 30, p. 4331-4334, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.05.022. Acesso em: 12 nov. 2024.
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      Andrade, L. H., Silva, A. V., & Pedrozo, E. C. (2009). First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B). Tetrahedron Letters, 50( 30), 4331-4334. doi:10.1016/j.tetlet.2009.05.022
    • NLM

      Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
    • Vancouver

      Andrade LH, Silva AV, Pedrozo EC. First dynamic kinetic resolution of selenium-containing chiral amines catalyzed by palladium (Pd/BaSO4) and Candida antartica lipase (CAL-B) [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4331-4334.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
  • 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: 12 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
    • NLM

      Cella R, Stefani HA. Ultrasound in heterocycles chemistry [Internet]. Tetrahedron. 2009 ; 65( 13): 2619-2641.[citado 2024 nov. 12 ] 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. 12 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: PROTEÍNAS, BIOQUÍMICA, PEPTÍDEOS (SÍNTESE)

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      PROTI, Patrícia Barrientos e MIRANDA, Maria Terêsa Machini de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, v. 49, n. 24, p. 3853-3857, 2008Tradução . . Acesso em: 12 nov. 2024.
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      Proti, P. B., & Miranda, M. T. M. de. (2008). 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters, 49( 24), 3853-3857.
    • NLM

      Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 nov. 12 ]
    • Vancouver

      Proti PB, Miranda MTM de. 'CA POT. 2+'-mediated thiolysis of peptide-resin linkage as an option for preparing protected peptide thioesters. Tetrahedron Letters. 2008 ;49( 24): 3853-3857.[citado 2024 nov. 12 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: TELÚRIO, REAGENTES ORGÂNICOS

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      PETRAGNANI, Nicola e MENDES, Samuel Rodrigues e SILVEIRA, Claudio da Cruz. Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, v. 49, n. 15, p. 2371-2372, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2008.02.085. Acesso em: 12 nov. 2024.
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      Petragnani, N., Mendes, S. R., & Silveira, C. da C. (2008). Tellurium tetrachloride: an improved method of preparation. Tetrahedron Letters, 49( 15), 2371-2372. doi:10.1016/j.tetlet.2008.02.085
    • NLM

      Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
    • Vancouver

      Petragnani N, Mendes SR, Silveira C da C. Tellurium tetrachloride: an improved method of preparation [Internet]. Tetrahedron Letters. 2008 ;49( 15): 2371-2372.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, TELÚRIO

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      OLIVEIRA, Roberta A. et al. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, v. 49, n. 40, p. 5759-5761, 2008Tradução . . Acesso em: 12 nov. 2024.
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      Oliveira, R. A., Oliveira, J. M., Rahmeier, L. H. S., Comasseto, J. V., Marino, J. P., & Menezes, P. H. (2008). Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, 49( 40), 5759-5761.
    • NLM

      Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 nov. 12 ]
    • Vancouver

      Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 nov. 12 ]
  • 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: 12 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. 12 ] 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. 12 ] 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: 12 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. 12 ] 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. 12 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: AMINAS (COMPOSTOS ORGÂNICOS), REAGENTES ORGÂNICOS

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      ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira. First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, v. 19, n. 10, p. 1175-1181, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.04.026. Acesso em: 12 nov. 2024.
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      Andrade, L. H., & Silva, A. V. (2008). First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, 19( 10), 1175-1181. doi:10.1016/j.tetasy.2008.04.026
    • NLM

      Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
    • Vancouver

      Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
  • 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: 12 nov. 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 nov. 12 ] 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. 12 ] 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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    • ABNT

      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: 12 nov. 2024.
    • APA

      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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.031
  • Source: Cell Calcium. Unidades: ICB, IQ

    Subjects: CARCINOMA, BIOQUÍMICA

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    • ABNT

      RESENDE, Rodrigo Ribeiro et al. Mechanism of acetylcholine-induced calcium signaling during neuronal differentiation of P19 embryonal carcinoma cells In vitro. Cell Calcium, v. 43, n. 2, p. 107-121, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.ceca.2007.04.007. Acesso em: 12 nov. 2024.
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      Resende, R. R., Gomes, K. N., Adhikari, A., Britto, L. R. G. de, & Ulrich, H. (2008). Mechanism of acetylcholine-induced calcium signaling during neuronal differentiation of P19 embryonal carcinoma cells In vitro. Cell Calcium, 43( 2), 107-121. doi:10.1016/j.ceca.2007.04.007
    • NLM

      Resende RR, Gomes KN, Adhikari A, Britto LRG de, Ulrich H. Mechanism of acetylcholine-induced calcium signaling during neuronal differentiation of P19 embryonal carcinoma cells In vitro [Internet]. Cell Calcium. 2008 ;43( 2): 107-121.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.ceca.2007.04.007
    • Vancouver

      Resende RR, Gomes KN, Adhikari A, Britto LRG de, Ulrich H. Mechanism of acetylcholine-induced calcium signaling during neuronal differentiation of P19 embryonal carcinoma cells In vitro [Internet]. Cell Calcium. 2008 ;43( 2): 107-121.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.ceca.2007.04.007
  • 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: 12 nov. 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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.083
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS

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    • ABNT

      TOLEDO, Fabiano Travanca et al. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, v. 49, n. 5, p. 873-875, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.169. Acesso em: 12 nov. 2024.
    • APA

      Toledo, F. T., Cunha, R. L. O. R., Raminelli, C., & Comasseto, J. V. (2008). Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, 49( 5), 873-875. doi:10.1016/j.tetlet.2007.11.169
    • NLM

      Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
    • Vancouver

      Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169

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