Filtros : "Indexado no Beilstein Database" "Indexado no Excerpta Medica" Removidos: "PORSANI, JORGE LUIS" "Clínica Médica" "ARANHAS" "ar" Limpar

Filtros



Refine with date range


  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: STAPHYLOCOCCUS (RESISTÊNCIA), DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, QUIMIOTERÁPICOS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PAULA, Fávero Reisdorfer et al. Molecular modeling studies and in vitro bioactivity evaluation of a set of novel 5-nitro-heterocyclic derivatives as anti-T. cruzi agents. Bioorganic & Medicinal Chemistry, v. 17, n. 7, p. 2673-2679, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2009.02.056. Acesso em: 14 nov. 2024.
    • APA

      Paula, F. R., Jorge, S. D., Almeida, L. V. de, Pasqualoto, K. F. M., & Tavares, L. C. (2009). Molecular modeling studies and in vitro bioactivity evaluation of a set of novel 5-nitro-heterocyclic derivatives as anti-T. cruzi agents. Bioorganic & Medicinal Chemistry, 17( 7), 2673-2679. doi:10.1016/j.bmc.2009.02.056
    • NLM

      Paula FR, Jorge SD, Almeida LV de, Pasqualoto KFM, Tavares LC. Molecular modeling studies and in vitro bioactivity evaluation of a set of novel 5-nitro-heterocyclic derivatives as anti-T. cruzi agents [Internet]. Bioorganic & Medicinal Chemistry. 2009 ; 17( 7): 2673-2679.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmc.2009.02.056
    • Vancouver

      Paula FR, Jorge SD, Almeida LV de, Pasqualoto KFM, Tavares LC. Molecular modeling studies and in vitro bioactivity evaluation of a set of novel 5-nitro-heterocyclic derivatives as anti-T. cruzi agents [Internet]. Bioorganic & Medicinal Chemistry. 2009 ; 17( 7): 2673-2679.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmc.2009.02.056
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 14 nov. 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 nov. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
  • Source: Tetrahedron Letters. Unidades: FCF, IQ

    Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 14 nov. 2024.
    • APA

      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. 14 ]
    • 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. 14 ]
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, POTÁSSIO, PALÁDIO

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
  • Source: Tetrahedron Letters. Unidade: FCF

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

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 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 nov. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
  • Source: Tetrahedron Asymmetry. Unidade: IQ

    Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
  • Source: Bioorganic and Medicinal Chemistry. Unidade: FCF

    Subjects: MODELAGEM MOLECULAR, STAPHYLOCOCCUS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.bmc.2009.03.011
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: PALÁDIO, CANDIDA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      SILVA JR., Luiz Fernando da e QUINTILIANO, Samir Augusto Pino. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, v. 50, n. 19, p. 2256-2260, 2009Tradução . . Acesso em: 14 nov. 2024.
    • APA

      Silva Jr., L. F. da, & Quintiliano, S. A. P. (2009). An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, 50( 19), 2256-2260.
    • NLM

      Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 nov. 14 ]
    • Vancouver

      Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 nov. 14 ]
  • Source: Bioorganic & Medicinal Chemistry. Unidade: FCF

    Subjects: BIODISPONIBILIDADE, FÁRMACOS, OLIGOSSACARÍDEOS

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ]
    • 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. 14 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: PROTEÍNAS, BIOQUÍMICA, PEPTÍDEOS (SÍNTESE)

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ]
    • 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. 14 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: TELÚRIO, REAGENTES ORGÂNICOS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2008.02.085
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, TELÚRIO

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ]
    • 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. 14 ]
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: QUÍMICA FARMACÊUTICA, TELÚRIO, REAÇÕES ORGÂNICAS

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetlet.2008.05.129
  • Source: Bioorganic and Medicinal Chemistry. Unidade: FCF

    Subjects: LEISHMANIA, FARMACOLOGIA, ANTIPROTOZOÁRIOS

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • 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: 14 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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.bmc.2008.05.076
  • Source: Tetrahedron. Unidade: FCF

    Subjects: POTÁSSIO (SÍNTESE), SÍNTESE ORGÂNICA

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tet.2008.05.085
  • Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, PEROXIDASE

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      MALVEZZI, Alberto et al. Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, v. 18, n. 1, p. 350-354, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2007.10.068. Acesso em: 14 nov. 2024.
    • APA

      Malvezzi, A., Rezende, L. de, Izidoro, M. A., Cezari, M. H. S., Juliano, L., & Amaral, A. T. do. (2008). Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, 18( 1), 350-354. doi:10.1016/j.bmcl.2007.10.068
    • NLM

      Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
    • Vancouver

      Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: AMINAS (COMPOSTOS ORGÂNICOS), REAGENTES ORGÂNICOS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 14 nov. 2024.
    • APA

      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. 14 ] 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. 14 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024