Filtros : "Indexado no Excerpta Medica" "QUÍMICA ORGÂNICA" Removidos: "BIOLOGIA" "FMRP-RBI" "Atlas" "Jornada Odontológica de Bauru" Limpar

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  • Source: Tetrahedron: Asymmetry. Unidade: FCFRP

    Assunto: QUÍMICA ORGÂNICA

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      BORGES, Keyller Bastos et al. Stereoselective biotransformations using fungi as biocatalysts. Tetrahedron: Asymmetry, v. 20, n. 4, p. 385-397, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.02.009. Acesso em: 13 jul. 2024.
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      Borges, K. B., Borges, W. de S., Durán-Patrón, R., Pupo, M. T., Bonato, P. S., & Collado, I. G. (2009). Stereoselective biotransformations using fungi as biocatalysts. Tetrahedron: Asymmetry, 20( 4), 385-397. doi:10.1016/j.tetasy.2009.02.009
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      Borges KB, Borges W de S, Durán-Patrón R, Pupo MT, Bonato PS, Collado IG. Stereoselective biotransformations using fungi as biocatalysts [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 4): 385-397.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2009.02.009
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      Borges KB, Borges W de S, Durán-Patrón R, Pupo MT, Bonato PS, Collado IG. Stereoselective biotransformations using fungi as biocatalysts [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 4): 385-397.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2009.02.009
  • 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: 13 jul. 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
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      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 jul. 13 ] 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 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: COMPOSTOS ORGANOMETÁLICOS, QUÍMICA ORGÂNICA

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      PRINCIVAL, Jefferson Luiz e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, v. 46, p. 6368-6371, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.08.097. Acesso em: 13 jul. 2024.
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      Princival, J. L., Santos, A. A. dos, & Comasseto, J. V. (2009). Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, 46, 6368-6371. doi:10.1016/j.tetlet.2009.08.097
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      Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
    • Vancouver

      Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
  • Source: Tetrahedron. Unidade: IQ

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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      COMASSETO, João Valdir e GARIANI, Rogério Aparecido. Biotransformations on organic selenides and tellurides: synthetic applications. Tetrahedron, v. 65, n. 41, p. 8447-8459, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2009.06.121. Acesso em: 13 jul. 2024.
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      Comasseto, J. V., & Gariani, R. A. (2009). Biotransformations on organic selenides and tellurides: synthetic applications. Tetrahedron, 65( 41), 8447-8459. doi:10.1016/j.tet.2009.06.121
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      Comasseto JV, Gariani RA. Biotransformations on organic selenides and tellurides: synthetic applications [Internet]. Tetrahedron. 2009 ; 65( 41): 8447-8459.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tet.2009.06.121
    • Vancouver

      Comasseto JV, Gariani RA. Biotransformations on organic selenides and tellurides: synthetic applications [Internet]. Tetrahedron. 2009 ; 65( 41): 8447-8459.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tet.2009.06.121
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      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: 13 jul. 2024.
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      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.
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      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 jul. 13 ]
    • 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 jul. 13 ]
  • Source: Canadian Journal of Chemical Engineering. Unidade: FCFRP

    Subjects: QUÍMICA ORGÂNICA, ANÁLISE ESPECTRAL

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      OLIVEIRA, Wanderley Pereira de et al. Evaluation of flow regimes in a semi-cylindrical spouted bed through statistical, mutual information, spectral and Hurst's analysis. Canadian Journal of Chemical Engineering, v. 86, n. 3, p. 582-597, 2008Tradução . . Disponível em: https://doi.org/10.1002/cjce.20055. Acesso em: 13 jul. 2024.
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      Oliveira, W. P. de, Souza, C. R. F., Lim, C. J., & Grace, J. R. (2008). Evaluation of flow regimes in a semi-cylindrical spouted bed through statistical, mutual information, spectral and Hurst's analysis. Canadian Journal of Chemical Engineering, 86( 3), 582-597. doi:10.1002/cjce.20055
    • NLM

      Oliveira WP de, Souza CRF, Lim CJ, Grace JR. Evaluation of flow regimes in a semi-cylindrical spouted bed through statistical, mutual information, spectral and Hurst's analysis [Internet]. Canadian Journal of Chemical Engineering. 2008 ; 86( 3): 582-597.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1002/cjce.20055
    • Vancouver

      Oliveira WP de, Souza CRF, Lim CJ, Grace JR. Evaluation of flow regimes in a semi-cylindrical spouted bed through statistical, mutual information, spectral and Hurst's analysis [Internet]. Canadian Journal of Chemical Engineering. 2008 ; 86( 3): 582-597.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1002/cjce.20055
  • Source: Plos Pathogens. Unidade: FCFRP

    Subjects: QUÍMICA ORGÂNICA, ASPERGILLUS, ANTI-HISTAMÍNICOS

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      MCDONAGH, Andrew et al. Sub-telomere directed gene expression during initiation of invasive aspergillosis. Plos Pathogens, v. 4, n. 9, p. e1000154-1-e1000154-21, 2008Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf. Acesso em: 13 jul. 2024.
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      McDonagh, A., Fedorova, N. D., Crabtree, J., Yu, Y., Kim, S., Chen, D., et al. (2008). Sub-telomere directed gene expression during initiation of invasive aspergillosis. Plos Pathogens, 4( 9), e1000154-1-e1000154-21. Recuperado de https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf
    • NLM

      McDonagh A, Fedorova ND, Crabtree J, Yu Y, Kim S, Chen D, Loss O, Cairns T, Goldman GH, Armstrong-James D, Haynes K, Haas H, Schretti M, May G, Nierman WC, Bignell E. Sub-telomere directed gene expression during initiation of invasive aspergillosis [Internet]. Plos Pathogens. 2008 ; 4( 9): e1000154-1-e1000154-21.[citado 2024 jul. 13 ] Available from: https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf
    • Vancouver

      McDonagh A, Fedorova ND, Crabtree J, Yu Y, Kim S, Chen D, Loss O, Cairns T, Goldman GH, Armstrong-James D, Haynes K, Haas H, Schretti M, May G, Nierman WC, Bignell E. Sub-telomere directed gene expression during initiation of invasive aspergillosis [Internet]. Plos Pathogens. 2008 ; 4( 9): e1000154-1-e1000154-21.[citado 2024 jul. 13 ] Available from: https://repositorio.usp.br/directbitstream/d8d32f07-bf55-44ca-9999-1050b34d7985/001705946.pdf
  • Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, PEROXIDASE

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      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: 13 jul. 2024.
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      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 jul. 13 ] 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 jul. 13 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
  • Source: Chemico-Biological Interactions. Unidade: IQSC

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA

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      CAVALCANTI, Bruno C. et al. Cytotoxic and genotoxic effects of tambjamine D, an alkaloid isolated from the nudibranch tambja eliora on Chinese hamster lung fibroblasts. Chemico-Biological Interactions, v. 1740, n. 3, p. 155-162, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.cbi.2008.05.029. Acesso em: 13 jul. 2024.
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      Cavalcanti, B. C., Júnior, H. V. N., Seleghim, M. H. R., Berlinck, R. G. de S., Cunha, G. M. A., Moraes, M. O., & Pessoa, C. (2008). Cytotoxic and genotoxic effects of tambjamine D, an alkaloid isolated from the nudibranch tambja eliora on Chinese hamster lung fibroblasts. Chemico-Biological Interactions, 1740( 3), 155-162. doi:10.1016/j.cbi.2008.05.029
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      Cavalcanti BC, Júnior HVN, Seleghim MHR, Berlinck RG de S, Cunha GMA, Moraes MO, Pessoa C. Cytotoxic and genotoxic effects of tambjamine D, an alkaloid isolated from the nudibranch tambja eliora on Chinese hamster lung fibroblasts [Internet]. Chemico-Biological Interactions. 2008 ; 1740( 3): 155-162.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.cbi.2008.05.029
    • Vancouver

      Cavalcanti BC, Júnior HVN, Seleghim MHR, Berlinck RG de S, Cunha GMA, Moraes MO, Pessoa C. Cytotoxic and genotoxic effects of tambjamine D, an alkaloid isolated from the nudibranch tambja eliora on Chinese hamster lung fibroblasts [Internet]. Chemico-Biological Interactions. 2008 ; 1740( 3): 155-162.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.cbi.2008.05.029
  • Source: Zeitschrift fuer Naturforschung. Section C. Unidade: FCFRP

    Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, QUÍMICA ORGÂNICA

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      LIÃO, luciano M et al. Trypanocidal activity of quinonemethide triterpenoids from cheiloclinium cognatum (hippocrateaceae). Zeitschrift fuer Naturforschung. Section C, v. 63c, n. 3-4, p. 207-210, 2008Tradução . . Acesso em: 13 jul. 2024.
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      Lião, luciano M., Silva , G. A., Monteiro, M. R., & Albuquerque, S. de. (2008). Trypanocidal activity of quinonemethide triterpenoids from cheiloclinium cognatum (hippocrateaceae). Zeitschrift fuer Naturforschung. Section C, 63c( 3-4), 207-210.
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      Lião luciano M, Silva GA, Monteiro MR, Albuquerque S de. Trypanocidal activity of quinonemethide triterpenoids from cheiloclinium cognatum (hippocrateaceae). Zeitschrift fuer Naturforschung. Section C. 2008 ; 63c( 3-4): 207-210.[citado 2024 jul. 13 ]
    • Vancouver

      Lião luciano M, Silva GA, Monteiro MR, Albuquerque S de. Trypanocidal activity of quinonemethide triterpenoids from cheiloclinium cognatum (hippocrateaceae). Zeitschrift fuer Naturforschung. Section C. 2008 ; 63c( 3-4): 207-210.[citado 2024 jul. 13 ]
  • Source: Neuropeptides. Unidades: FMRP, FFCLRP

    Subjects: QUÍMICA ORGÂNICA, NEUROQUÍMICA

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      BASSI, Gabriel S. et al. Anxiogenic effects of activation of NK-1 receptors of the dorsal periaqueductal gray as assessed by the elevated plus-maze, ultrasound vocalizations and tail-flick tests. Neuropeptides, v. 41, n. 6, p. 365-374, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.npep.2007.09.004. Acesso em: 13 jul. 2024.
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      Bassi, G. S., Nobre, M. J., Araújo, J. E. de, & Brandão, M. L. (2007). Anxiogenic effects of activation of NK-1 receptors of the dorsal periaqueductal gray as assessed by the elevated plus-maze, ultrasound vocalizations and tail-flick tests. Neuropeptides, 41( 6), 365-374. doi:10.1016/j.npep.2007.09.004
    • NLM

      Bassi GS, Nobre MJ, Araújo JE de, Brandão ML. Anxiogenic effects of activation of NK-1 receptors of the dorsal periaqueductal gray as assessed by the elevated plus-maze, ultrasound vocalizations and tail-flick tests [Internet]. Neuropeptides. 2007 ; 41( 6): 365-374.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.npep.2007.09.004
    • Vancouver

      Bassi GS, Nobre MJ, Araújo JE de, Brandão ML. Anxiogenic effects of activation of NK-1 receptors of the dorsal periaqueductal gray as assessed by the elevated plus-maze, ultrasound vocalizations and tail-flick tests [Internet]. Neuropeptides. 2007 ; 41( 6): 365-374.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.npep.2007.09.004
  • Source: Journal of the Chilean Chemical Society. Unidade: FCFRP

    Assunto: QUÍMICA ORGÂNICA

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      VENEZIANI, Rodrigo C. S. et al. In vitro trypanocidal activity and chemical constituents of Aspilia platyphylla (baker) blake. Journal of the Chilean Chemical Society, v. 52, n. 1, p. 1092-1094, 2007Tradução . . Disponível em: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100008&lng=pt&nrm=iso&tlng=en. Acesso em: 13 jul. 2024.
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      Veneziani, R. C. S., Oliveira, D. C. R. de, Albuquerque, S. de, & Cunha, W. R. (2007). In vitro trypanocidal activity and chemical constituents of Aspilia platyphylla (baker) blake. Journal of the Chilean Chemical Society, 52( 1), 1092-1094. Recuperado de http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100008&lng=pt&nrm=iso&tlng=en
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      Veneziani RCS, Oliveira DCR de, Albuquerque S de, Cunha WR. In vitro trypanocidal activity and chemical constituents of Aspilia platyphylla (baker) blake [Internet]. Journal of the Chilean Chemical Society. 2007 ; 52( 1): 1092-1094.[citado 2024 jul. 13 ] Available from: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100008&lng=pt&nrm=iso&tlng=en
    • Vancouver

      Veneziani RCS, Oliveira DCR de, Albuquerque S de, Cunha WR. In vitro trypanocidal activity and chemical constituents of Aspilia platyphylla (baker) blake [Internet]. Journal of the Chilean Chemical Society. 2007 ; 52( 1): 1092-1094.[citado 2024 jul. 13 ] Available from: http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000100008&lng=pt&nrm=iso&tlng=en
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      TOLEDO, Fabiano Travanca et al. The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, v. 48, n. 46, p. 8125-8127, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.09.111. Acesso em: 13 jul. 2024.
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      Toledo, F. T., Marques, H., Comasseto, J. V., & Raminelli, C. (2007). The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, 48( 46), 8125-8127. doi:10.1016/j.tetlet.2007.09.111
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      Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
    • Vancouver

      Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA

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      MARZORATI, Liliana et al. New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, v. 48, n. 37, p. 6509-6513, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.07.054. Acesso em: 13 jul. 2024.
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      Marzorati, L., Barazzone, G. C., Bueno Filho, M. A., Wladislaw, B., & Di Vitta, C. (2007). New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, 48( 37), 6509-6513. doi:10.1016/j.tetlet.2007.07.054
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      Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
    • Vancouver

      Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TELÚRIO, LÍTIO

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      DOS SANTOS, Alcindo Aparecido et al. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, v. 47, n. 50, p. 8933-8935, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.10.039. Acesso em: 13 jul. 2024.
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      Dos Santos, A. A., Ferrarini, R. dos S., Princival, J. L., & Comasseto, J. V. (2006). Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, 47( 50), 8933-8935. doi:10.1016/j.tetlet.2006.10.039
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      Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
    • Vancouver

      Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: LIPASE, QUÍMICA ORGÂNICA

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      DOS SANTOS, Alcindo Aparecido et al. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, v. 17, n. 15, p. 2252-2259, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.024. Acesso em: 13 jul. 2024.
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      Dos Santos, A. A., Da Costa, C. E., Princival, J. L., & Comasseto, J. V. (2006). Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, 17( 15), 2252-2259. doi:10.1016/j.tetasy.2006.07.024
    • NLM

      Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
    • Vancouver

      Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, QUÍMICA ORGÂNICA

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      VIEIRA, Tiago de Oliveira et al. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 17, n. 13, p. 1990-1994, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.014. Acesso em: 13 jul. 2024.
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      Vieira, T. de O., Ferraz, H. M. C., Andrade, L. H., & Porto, A. L. M. (2006). Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 17( 13), 1990-1994. doi:10.1016/j.tetasy.2006.07.014
    • NLM

      Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
    • Vancouver

      Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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    • ABNT

      NIHEI, Ken-ichi et al. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, v. 62, n. 35, p. 8335-8350, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.06.051. Acesso em: 13 jul. 2024.
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      Nihei, K. -ichi, Kato, M. J., Yamane, T., & Konno, K. (2006). An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, 62( 35), 8335-8350. doi:10.1016/j.tet.2006.06.051
    • NLM

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
    • Vancouver

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
  • Source: Basic and Clinical Pharmacology & Toxicology. Unidade: FCFRP

    Subjects: ANTI-INFLAMATÓRIOS, TOXICOLOGIA, MITOCÔNDRIAS, QUÍMICA ORGÂNICA

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      LEITE, Samara et al. Mitocrondrial uncoupling by the sulindac metabolite, sulindac sulfide. Basic and Clinical Pharmacology & Toxicology, v. 99, p. 294-299, 2006Tradução . . Acesso em: 13 jul. 2024.
    • APA

      Leite, S., Martins, N. M., Dorta, D. J., Curti, C., Uyemura, S. A., & Santos, A. C. dos. (2006). Mitocrondrial uncoupling by the sulindac metabolite, sulindac sulfide. Basic and Clinical Pharmacology & Toxicology, 99, 294-299.
    • NLM

      Leite S, Martins NM, Dorta DJ, Curti C, Uyemura SA, Santos AC dos. Mitocrondrial uncoupling by the sulindac metabolite, sulindac sulfide. Basic and Clinical Pharmacology & Toxicology. 2006 ; 99 294-299.[citado 2024 jul. 13 ]
    • Vancouver

      Leite S, Martins NM, Dorta DJ, Curti C, Uyemura SA, Santos AC dos. Mitocrondrial uncoupling by the sulindac metabolite, sulindac sulfide. Basic and Clinical Pharmacology & Toxicology. 2006 ; 99 294-299.[citado 2024 jul. 13 ]
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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    • ABNT

      GARIANI, Rogério Aparecido et al. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination. Tetrahedron - Asymmetry, v. 17, n. 20, p. 2930-2934, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.10.034. Acesso em: 13 jul. 2024.
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      Gariani, R. A., Simonelli, F., Oliveira, A. R. M. de, Barison, A., & Comasseto, J. V. (2006). A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination. Tetrahedron - Asymmetry, 17( 20), 2930-2934. doi:10.1016/j.tetasy.2006.10.034
    • NLM

      Gariani RA, Simonelli F, Oliveira ARM de, Barison A, Comasseto JV. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 20): 2930-2934.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.10.034
    • Vancouver

      Gariani RA, Simonelli F, Oliveira ARM de, Barison A, Comasseto JV. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 20): 2930-2934.[citado 2024 jul. 13 ] Available from: https://doi.org/10.1016/j.tetasy.2006.10.034

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