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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: 07 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. 07 ] 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. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
  • Source: Drug Discovery Today. Unidades: IQ, IFSC

    Subjects: SCHISTOSOMA MANSONI, VACINAS

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      DE MARCO, Ricardo e VERJOVSKI-ALMEIDA, Sergio. Schistosomes: proteomics studies for potential novel vaccines and drug targets. Drug Discovery Today, v. 14, n. 9/10, p. 472-478, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.drudis.2009.01.011. Acesso em: 07 nov. 2024.
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      De Marco, R., & Verjovski-Almeida, S. (2009). Schistosomes: proteomics studies for potential novel vaccines and drug targets. Drug Discovery Today, 14( 9/10), 472-478. doi:10.1016/j.drudis.2009.01.011
    • NLM

      De Marco R, Verjovski-Almeida S. Schistosomes: proteomics studies for potential novel vaccines and drug targets [Internet]. Drug Discovery Today. 2009 ; 14( 9/10): 472-478.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.drudis.2009.01.011
    • Vancouver

      De Marco R, Verjovski-Almeida S. Schistosomes: proteomics studies for potential novel vaccines and drug targets [Internet]. Drug Discovery Today. 2009 ; 14( 9/10): 472-478.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.drudis.2009.01.011
  • Source: Materials Research Bulletin. Unidade: IQ

    Subjects: MATERIAIS COMPÓSITOS, ELETROQUÍMICA

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      ROCHA, Michele Aparecida et al. Preparation and characterization of colloidal Ni'(OH) IND. 2'/bentonite composites. Materials Research Bulletin, v. 44, n. 5, p. 970-976, 2009Tradução . . Acesso em: 07 nov. 2024.
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      Rocha, M. A., Anaissi, F. J., Toma, H. E., Araki, K., & Winnischofer, H. (2009). Preparation and characterization of colloidal Ni'(OH) IND. 2'/bentonite composites. Materials Research Bulletin, 44( 5), 970-976.
    • NLM

      Rocha MA, Anaissi FJ, Toma HE, Araki K, Winnischofer H. Preparation and characterization of colloidal Ni'(OH) IND. 2'/bentonite composites. Materials Research Bulletin. 2009 ; 44( 5): 970-976.[citado 2024 nov. 07 ]
    • Vancouver

      Rocha MA, Anaissi FJ, Toma HE, Araki K, Winnischofer H. Preparation and characterization of colloidal Ni'(OH) IND. 2'/bentonite composites. Materials Research Bulletin. 2009 ; 44( 5): 970-976.[citado 2024 nov. 07 ]
  • Source: Synthesis. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TÁLIO, NITRATOS, CARBONO

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      FERRAZ, Helena Maria Carvalho e CARNEIRO, Vânia Maria Teixeira e SILVA JUNIOR, Luiz Fernando da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, n. 3, p. 385-388, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf. Acesso em: 07 nov. 2024.
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      Ferraz, H. M. C., Carneiro, V. M. T., & Silva Junior, L. F. da. (2009). Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, ( 3), 385-388. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
    • NLM

      Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 nov. 07 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
    • Vancouver

      Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 nov. 07 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
  • 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: 07 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. 07 ]
    • 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. 07 ]
  • 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: 07 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. 07 ] 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. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      SILVA, Márcio S. e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, v. 50, n. 47, p. 6498-6501, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.09.023. Acesso em: 07 nov. 2024.
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      Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, 50( 47), 6498-6501. doi:10.1016/j.tetlet.2009.09.023
    • NLM

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
    • Vancouver

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
  • 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: 07 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. 07 ] 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. 07 ] 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: 07 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. 07 ] 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. 07 ] 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: 07 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. 07 ] 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. 07 ] 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: 07 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. 07 ] 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. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
  • Source: Enzyme and Microbial Technology. Unidade: FCF

    Subjects: STREPTOMYCES, FERMENTAÇÃO

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      MARQUES, Daniela de Araújo Viana et al. Kinetic and thermodynamic investigation on clavulanic acid formation and degradation during glycerol fermentation by Streptomyces DAUFPE 3060. Enzyme and Microbial Technology, v. 45, n. 2, p. 169-173, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2009.03.005. Acesso em: 07 nov. 2024.
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      Marques, D. de A. V., Oliveira, R. P. de S., Perego, P., Porto, A. L. F., Pessoa Junior, A., & Converti, A. (2009). Kinetic and thermodynamic investigation on clavulanic acid formation and degradation during glycerol fermentation by Streptomyces DAUFPE 3060. Enzyme and Microbial Technology, 45( 2), 169-173. doi:10.1016/j.enzmictec.2009.03.005
    • NLM

      Marques D de AV, Oliveira RP de S, Perego P, Porto ALF, Pessoa Junior A, Converti A. Kinetic and thermodynamic investigation on clavulanic acid formation and degradation during glycerol fermentation by Streptomyces DAUFPE 3060 [Internet]. Enzyme and Microbial Technology. 2009 ; 45( 2): 169-173.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.enzmictec.2009.03.005
    • Vancouver

      Marques D de AV, Oliveira RP de S, Perego P, Porto ALF, Pessoa Junior A, Converti A. Kinetic and thermodynamic investigation on clavulanic acid formation and degradation during glycerol fermentation by Streptomyces DAUFPE 3060 [Internet]. Enzyme and Microbial Technology. 2009 ; 45( 2): 169-173.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.enzmictec.2009.03.005
  • Source: Journal of Molecular Graphics and Modelling. Unidades: IFSC, FCF

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

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      TROSSINI, Gustavo Henrique Goulart et al. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies. Journal of Molecular Graphics and Modelling, v. 28, n. 1, p. 3-11, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jmgm.2009.03.001. Acesso em: 07 nov. 2024.
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      Trossini, G. H. G., Guido, R. V. C., Oliva, G., Ferreira, E. I., & Andricopulo, A. D. (2009). Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies. Journal of Molecular Graphics and Modelling, 28( 1), 3-11. doi:10.1016/j.jmgm.2009.03.001
    • NLM

      Trossini GHG, Guido RVC, Oliva G, Ferreira EI, Andricopulo AD. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies [Internet]. Journal of Molecular Graphics and Modelling. 2009 ; 28( 1): 3-11.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.jmgm.2009.03.001
    • Vancouver

      Trossini GHG, Guido RVC, Oliva G, Ferreira EI, Andricopulo AD. Quantitative structure-activity relationships for a series of inhibitors of cruzain from Trypanosoma cruzi: molecular modeling, CoMFA and CoMSIA studies [Internet]. Journal of Molecular Graphics and Modelling. 2009 ; 28( 1): 3-11.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.jmgm.2009.03.001
  • 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: 07 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. 07 ] 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. 07 ] Available from: https://doi.org/10.1016/j.tetlet.2009.05.022
  • Source: Dental Materials. Unidades: IQ, FO

    Subjects: MATERIAIS COMPÓSITOS, SOLVENTE

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      PFEIFER, Carmem Silvia Costa et al. Bis-GMA co-polymerizations: influence on conversion, flexural properties, fracture toughness and susceptibility to ethanol degradation of experimental composites. Dental Materials, v. 25, n. 9, p. 1136-1141, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.dental.2009.03.010. Acesso em: 07 nov. 2024.
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      Pfeifer, C. S. C., Silva, L. R., Kawano, Y., & Braga, R. R. (2009). Bis-GMA co-polymerizations: influence on conversion, flexural properties, fracture toughness and susceptibility to ethanol degradation of experimental composites. Dental Materials, 25( 9), 1136-1141. doi:10.1016/j.dental.2009.03.010
    • NLM

      Pfeifer CSC, Silva LR, Kawano Y, Braga RR. Bis-GMA co-polymerizations: influence on conversion, flexural properties, fracture toughness and susceptibility to ethanol degradation of experimental composites [Internet]. Dental Materials. 2009 ; 25( 9): 1136-1141.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.dental.2009.03.010
    • Vancouver

      Pfeifer CSC, Silva LR, Kawano Y, Braga RR. Bis-GMA co-polymerizations: influence on conversion, flexural properties, fracture toughness and susceptibility to ethanol degradation of experimental composites [Internet]. Dental Materials. 2009 ; 25( 9): 1136-1141.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.dental.2009.03.010
  • 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: 07 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. 07 ] 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. 07 ] Available from: https://doi.org/10.1016/j.tet.2008.12.027
  • Source: Neurobiology of Aging. Unidade: IQ

    Subjects: DOENÇA DE ALZHEIMER, ESTRESSE OXIDATIVO, DANO AO DNA

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      WEISSMAN, Lior et al. DNA base excision repair activities in mouse models of Alzheimer's disease. Neurobiology of Aging, v. 30, n. 12, p. 2080-2081, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.neurobiolaging.2008.02.014. Acesso em: 07 nov. 2024.
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      Weissman, L., Souza-Pinto, N. C. de, Mattson, M. P., & Bohr, V. A. (2009). DNA base excision repair activities in mouse models of Alzheimer's disease. Neurobiology of Aging, 30( 12), 2080-2081. doi:10.1016/j.neurobiolaging.2008.02.014
    • NLM

      Weissman L, Souza-Pinto NC de, Mattson MP, Bohr VA. DNA base excision repair activities in mouse models of Alzheimer's disease [Internet]. Neurobiology of Aging. 2009 ; 30( 12): 2080-2081.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2008.02.014
    • Vancouver

      Weissman L, Souza-Pinto NC de, Mattson MP, Bohr VA. DNA base excision repair activities in mouse models of Alzheimer's disease [Internet]. Neurobiology of Aging. 2009 ; 30( 12): 2080-2081.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2008.02.014
  • 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: 07 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. 07 ]
    • 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. 07 ]
  • 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: 07 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. 07 ] 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. 07 ] 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: 07 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. 07 ]
    • 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. 07 ]

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