Filtros : "Tetrahedron" "FCFRP-602" Removido: "IFSC" Limpar

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  • Source: Tetrahedron. Unidades: FCFRP, FMRP

    Subjects: TRIPANOSSOMICIDAS, TRYPANOSOMA CRUZI, MACRÓFAGOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      CAMPO, Vanessa Leiria et al. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, v. 71, n. 39, p. 7344–7353, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2015.04.085. Acesso em: 24 ago. 2024.
    • APA

      Campo, V. L., Ivanova, I. M., Carvalho, I., Lopes, C. D., Carneiro, Z., Saalbach, G., et al. (2015). Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, 71( 39), 7344–7353. doi:10.1016/j.tet.2015.04.085
    • NLM

      Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2015.04.085
    • Vancouver

      Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2015.04.085
  • Source: Tetrahedron. Unidades: FCFRP, FMRP

    Subjects: TRIPANOSSOMICIDAS, TECNOLOGIA FARMACÊUTICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      GALANTE, Eva et al. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity. Tetrahedron, v. 67, n. 33, p. 5902-5912, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2011.06.065. Acesso em: 24 ago. 2024.
    • APA

      Galante, E., Geraci, C., Sciuto, S., Campo, V. L., Carvalho, I., Sesti-Costa, R., et al. (2011). Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity. Tetrahedron, 67( 33), 5902-5912. doi:10.1016/j.tet.2011.06.065
    • NLM

      Galante E, Geraci C, Sciuto S, Campo VL, Carvalho I, Sesti-Costa R, Guedes PM da M, Silva JS da, Hill L, Nepogodiev SA, Field RA. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity [Internet]. Tetrahedron. 2011 ; 67( 33): 5902-5912.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2011.06.065
    • Vancouver

      Galante E, Geraci C, Sciuto S, Campo VL, Carvalho I, Sesti-Costa R, Guedes PM da M, Silva JS da, Hill L, Nepogodiev SA, Field RA. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity [Internet]. Tetrahedron. 2011 ; 67( 33): 5902-5912.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2011.06.065
  • Source: Tetrahedron. Unidade: FCFRP

    Subjects: SÍNTESE QUÍMICA, FÁRMACOS

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    • ABNT

      LEONETI, Valquiria Aragão et al. Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis. Tetrahedron, v. 66, n. 49, p. 9475-9492, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2010.10.001. Acesso em: 24 ago. 2024.
    • APA

      Leoneti, V. A., Campo, V. L., Gomes, A. da S., Field, R. A., & Carvalho, I. (2010). Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis. Tetrahedron, 66( 49), 9475-9492. doi:10.1016/j.tet.2010.10.001
    • NLM

      Leoneti VA, Campo VL, Gomes A da S, Field RA, Carvalho I. Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis [Internet]. Tetrahedron. 2010 ; 66( 49): 9475-9492.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2010.10.001
    • Vancouver

      Leoneti VA, Campo VL, Gomes A da S, Field RA, Carvalho I. Application of copper(I)-catalysed azide/alkyne cycloaddition (CuAAC) 'click chemistry' in carbohydrate drug and neoglycopolymer synthesis [Internet]. Tetrahedron. 2010 ; 66( 49): 9475-9492.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2010.10.001
  • Source: Tetrahedron. Unidade: FCFRP

    Subjects: PEPTÍDEOS CÍCLICOS, QUÍMICA MÉDICA

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    • ABNT

      MARTINS, Maristela B. e CARVALHO, Ivone. Diketopiperazines: biological activity and synthesis. Tetrahedron, v. 63, n. 40, p. 9923-9932, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.04.105. Acesso em: 24 ago. 2024.
    • APA

      Martins, M. B., & Carvalho, I. (2007). Diketopiperazines: biological activity and synthesis. Tetrahedron, 63( 40), 9923-9932. doi:10.1016/j.tet.2007.04.105
    • NLM

      Martins MB, Carvalho I. Diketopiperazines: biological activity and synthesis [Internet]. Tetrahedron. 2007 ; 63( 40): 9923-9932.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2007.04.105
    • Vancouver

      Martins MB, Carvalho I. Diketopiperazines: biological activity and synthesis [Internet]. Tetrahedron. 2007 ; 63( 40): 9923-9932.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tet.2007.04.105
  • Source: Tetrahedron. Unidade: FCFRP

    Subjects: ENZIMAS GLICOLÍTICAS, INIBIDORES DE ENZIMAS

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    • ABNT

      MELO, Eduardo Borges de e GOMES, Adriane da Silveira e CARVALHO, Ivone. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron, v. 62, n. 44, p. 10277-10302, 2006Tradução . . Acesso em: 24 ago. 2024.
    • APA

      Melo, E. B. de, Gomes, A. da S., & Carvalho, I. (2006). 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron, 62( 44), 10277-10302.
    • NLM

      Melo EB de, Gomes A da S, Carvalho I. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron. 2006 ; 62( 44): 10277-10302.[citado 2024 ago. 24 ]
    • Vancouver

      Melo EB de, Gomes A da S, Carvalho I. 'alfa' and 'beta' Glucosidase inhibitors: chemical structure and biological activity. Tetrahedron. 2006 ; 62( 44): 10277-10302.[citado 2024 ago. 24 ]
  • Source: Tetrahedron. Unidades: FFCLRP, FCFRP

    Assunto: FÁRMACOS (QUÍMICA)

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    • ABNT

      DONATE, Paulo Marcos et al. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, v. 14, p. 3253-3256, 2003Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2003.08.031. Acesso em: 24 ago. 2024.
    • APA

      Donate, P. M., Frederico, D., Silva, R. da, Constantino, M. G., Del Ponte, G., & Bonatto, P. S. (2003). Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, 14, 3253-3256. doi:10.1016/j.tetasy.2003.08.031
    • NLM

      Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031
    • Vancouver

      Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031

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