Filtros : "Indexado no Science Citation Index" "Carvalho, Ivone" "FCFRP" Removidos: "Indexado no : CAB Abstracts" "SD" "SHUHAMA, TADAO" Limpar

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  • Fonte: Carbohydrate Polymers. Unidade: FCFRP

    Assuntos: CARRAGENINA, FARMACOLOGIA

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      CAMPO, Vanessa Leiria et al. Carrageenans: biological properties, chemical modifications and structural analysis - a review. Carbohydrate Polymers, v. 77, n. 2, p. 167-180, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2009.01.020. Acesso em: 18 nov. 2024.
    • APA

      Campo, V. L., Kawano, D. F., Silva Junior, D. B. da, & Carvalho, I. (2009). Carrageenans: biological properties, chemical modifications and structural analysis - a review. Carbohydrate Polymers, 77( 2), 167-180. doi:10.1016/j.carbpol.2009.01.020
    • NLM

      Campo VL, Kawano DF, Silva Junior DB da, Carvalho I. Carrageenans: biological properties, chemical modifications and structural analysis - a review [Internet]. Carbohydrate Polymers. 2009 ; 77( 2): 167-180.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.carbpol.2009.01.020
    • Vancouver

      Campo VL, Kawano DF, Silva Junior DB da, Carvalho I. Carrageenans: biological properties, chemical modifications and structural analysis - a review [Internet]. Carbohydrate Polymers. 2009 ; 77( 2): 167-180.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.carbpol.2009.01.020
  • Fonte: Journal of Physical Chemistry Part A. Unidade: FCFRP

    Assuntos: QUÍMICA FARMACÊUTICA, NEOPLASIAS (TERAPIA)

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    • ABNT

      SILVA, Vinicius Barreto da et al. Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A, v. 112, n. 38, p. 8902-8910, 2008Tradução . . Acesso em: 18 nov. 2024.
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      Silva, V. B. da, Kawano, D. F., Gomes, A. da S., Carvalho, I., Taft, C. A., & Silva, C. H. T. de P. da. (2008). Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A, 112( 38), 8902-8910.
    • NLM

      Silva VB da, Kawano DF, Gomes A da S, Carvalho I, Taft CA, Silva CHT de P da. Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A. 2008 ; 112( 38): 8902-8910.[citado 2024 nov. 18 ]
    • Vancouver

      Silva VB da, Kawano DF, Gomes A da S, Carvalho I, Taft CA, Silva CHT de P da. Molecular dynamics, density functional, ADMET predictions, virtual screening, and molecular interaction field studies for identification and evaluation of novel potential CDK2 inhibitors in cancer therapy. Journal of Physical Chemistry Part A. 2008 ; 112( 38): 8902-8910.[citado 2024 nov. 18 ]
  • Fonte: Tetrahedron. Unidade: FCFRP

    Assuntos: PEPTÍDEOS CÍCLICOS, QUÍMICA MÉDICA

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      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: 18 nov. 2024.
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      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 nov. 18 ] 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 nov. 18 ] Available from: https://doi.org/10.1016/j.tet.2007.04.105
  • Fonte: Current Medical Chemistry. Unidade: FCFRP

    Assuntos: ANTIBIÓTICOS, HIV

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      SILVA, Julierme G. da e CARVALHO, Ivone. New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry, v. 14, p. 1101-1119, 2007Tradução . . Acesso em: 18 nov. 2024.
    • APA

      Silva, J. G. da, & Carvalho, I. (2007). New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry, 14, 1101-1119.
    • NLM

      Silva JG da, Carvalho I. New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry. 2007 ; 14 1101-1119.[citado 2024 nov. 18 ]
    • Vancouver

      Silva JG da, Carvalho I. New insights into aminoglycoside antibiotics and derivatives. Current Medical Chemistry. 2007 ; 14 1101-1119.[citado 2024 nov. 18 ]
  • Fonte: Organic and Biomolecular Chemistry. Unidade: FCFRP

    Assuntos: GLICOPEPTÍDEOS, TRYPANOSOMA CRUZI

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      CAMPO, Vanessa Leiria et al. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins. Organic and Biomolecular Chemistry, v. 5, p. 2645-2657, 2007Tradução . . Disponível em: https://doi.org/10.1039/b707772f. Acesso em: 18 nov. 2024.
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      Campo, V. L., Carvalho, I., Allman, S., Davis, B. G., & Field, R. A. (2007). Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins. Organic and Biomolecular Chemistry, 5, 2645-2657. doi:10.1039/b707772f
    • NLM

      Campo VL, Carvalho I, Allman S, Davis BG, Field RA. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins [Internet]. Organic and Biomolecular Chemistry. 2007 ; 5 2645-2657.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1039/b707772f
    • Vancouver

      Campo VL, Carvalho I, Allman S, Davis BG, Field RA. Chemical and chemoenzymatic synthesis of glycosyl-amino acids and glycopeptides related to Trypanosoma cruzi mucins [Internet]. Organic and Biomolecular Chemistry. 2007 ; 5 2645-2657.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1039/b707772f
  • Fonte: Química Niva. Unidade: FCFRP

    Assuntos: HIPERLIPIDEMIA, FÁRMACOS

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    • ABNT

      CAMPO, Vanessa Leiria e CARVALHO, Ivone. Estatinas hipolipêmicas e novas tendências terapêuticas. Química Niva, v. 30, n. 2, p. 425-430, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0100-40422007000200033. Acesso em: 18 nov. 2024.
    • APA

      Campo, V. L., & Carvalho, I. (2007). Estatinas hipolipêmicas e novas tendências terapêuticas. Química Niva, 30( 2), 425-430. doi:10.1590/s0100-40422007000200033
    • NLM

      Campo VL, Carvalho I. Estatinas hipolipêmicas e novas tendências terapêuticas [Internet]. Química Niva. 2007 ; 30( 2): 425-430.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0100-40422007000200033
    • Vancouver

      Campo VL, Carvalho I. Estatinas hipolipêmicas e novas tendências terapêuticas [Internet]. Química Niva. 2007 ; 30( 2): 425-430.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0100-40422007000200033
  • Fonte: Toxicon. Unidade: FCFRP

    Assuntos: CROTALÁRIA, CITOTOXINAS

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    • ABNT

      MINGATTO, Fábio E. et al. Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline. Toxicon, v. 50, n. 5, p. 724-730, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2007.06.006. Acesso em: 18 nov. 2024.
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      Mingatto, F. E., Dorta, D. J., Santos, A. B. dos, Carvalho, I., Silva, C. H. T. P. da, Silva, V. B. da, et al. (2007). Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline. Toxicon, 50( 5), 724-730. doi:10.1016/j.toxicon.2007.06.006
    • NLM

      Mingatto FE, Dorta DJ, Santos AB dos, Carvalho I, Silva CHTP da, Silva VB da, Uyemura SA, Santos AC dos, Curti C. Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline [Internet]. Toxicon. 2007 ; 50( 5): 724-730.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.toxicon.2007.06.006
    • Vancouver

      Mingatto FE, Dorta DJ, Santos AB dos, Carvalho I, Silva CHTP da, Silva VB da, Uyemura SA, Santos AC dos, Curti C. Dehydromonocrotaline inhibits mitochondrial complex I.: a potencial mechanism accounting for hepatotoxicity of monocrotaline [Internet]. Toxicon. 2007 ; 50( 5): 724-730.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.toxicon.2007.06.006
  • Fonte: Journal of Brazilian Chemical Society. Unidade: FCFRP

    Assuntos: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, AMINOÁCIDOS, GLICOSÍDEOS

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    • ABNT

      CAMPO, Vanessa Leiria e BORGES, Áurea Donizete Lanchote e CARVALHO, Ivone. HPLC analysis of glycosylated amino acids. Journal of Brazilian Chemical Society, v. 17, n. 4, p. 648-654, 2006Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532006000400004. Acesso em: 18 nov. 2024.
    • APA

      Campo, V. L., Borges, Á. D. L., & Carvalho, I. (2006). HPLC analysis of glycosylated amino acids. Journal of Brazilian Chemical Society, 17( 4), 648-654. doi:10.1590/s0103-50532006000400004
    • NLM

      Campo VL, Borges ÁDL, Carvalho I. HPLC analysis of glycosylated amino acids [Internet]. Journal of Brazilian Chemical Society. 2006 ; 17( 4): 648-654.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0103-50532006000400004
    • Vancouver

      Campo VL, Borges ÁDL, Carvalho I. HPLC analysis of glycosylated amino acids [Internet]. Journal of Brazilian Chemical Society. 2006 ; 17( 4): 648-654.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0103-50532006000400004
  • Fonte: Tetrahedron. Unidade: FCFRP

    Assuntos: 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: 18 nov. 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 nov. 18 ]
    • 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 nov. 18 ]
  • Fonte: Bioorganic and Medicinal Chemistry. Unidades: IQ, FCFRP

    Assuntos: ANTIPARASITÁRIOS, PRODUTOS NATURAIS, TRYPANOSOMA CRUZI

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    • ABNT

      BERNARDES, Lilian Sibelle Campos et al. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, v. 14, p. 7075-7082, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2006.07.006. Acesso em: 18 nov. 2024.
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      Bernardes, L. S. C., Kato, M. J., Albuquerque, S. de, & Carvalho, I. (2006). Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol. Bioorganic and Medicinal Chemistry, 14, 7075-7082. doi:10.1016/j.bmc.2006.07.006
    • NLM

      Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
    • Vancouver

      Bernardes LSC, Kato MJ, Albuquerque S de, Carvalho I. Synthesis and trypanocidal activity of 1,4-bis(3,4,5-trimethoxy-phenyl)-1,4-butanediol and 1,4-bis-(3,4-dimethoxyphenyl)-1,4-butanediol [Internet]. Bioorganic and Medicinal Chemistry. 2006 ; 14 7075-7082.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bmc.2006.07.006
  • Fonte: Journal of Molecular Graphics and Modelling. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      SILVA, Carlos H. T. P. da et al. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease. Journal of Molecular Graphics and Modelling, v. 25, p. 169-175, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jmgm.2005.12.002. Acesso em: 18 nov. 2024.
    • APA

      Silva, C. H. T. P. da, Campo, V. L., Carvalho, I., & Taft, C. A. (2006). Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease. Journal of Molecular Graphics and Modelling, 25, 169-175. doi:10.1016/j.jmgm.2005.12.002
    • NLM

      Silva CHTP da, Campo VL, Carvalho I, Taft CA. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease [Internet]. Journal of Molecular Graphics and Modelling. 2006 ; 25 169-175.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.jmgm.2005.12.002
    • Vancouver

      Silva CHTP da, Campo VL, Carvalho I, Taft CA. Molecular modeling, docking and ADMET studies applied to the design of a novel hybrid for treatment of Alzheimer's disease [Internet]. Journal of Molecular Graphics and Modelling. 2006 ; 25 169-175.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.jmgm.2005.12.002
  • Fonte: Journal of Brazilian Chemical Society. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      FURTADO, Niege Araçari Jacometti Cardoso et al. Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain. Journal of Brazilian Chemical Society, v. 16, n. 6B, p. 1448-1453, 2005Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532005000800026. Acesso em: 18 nov. 2024.
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      Furtado, N. A. J. C., Pupo, M. T., Carvalho, I., Campo, V. L., Duarte, M. C. T., & Bastos, J. K. (2005). Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain. Journal of Brazilian Chemical Society, 16( 6B), 1448-1453. doi:10.1590/s0103-50532005000800026
    • NLM

      Furtado NAJC, Pupo MT, Carvalho I, Campo VL, Duarte MCT, Bastos JK. Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain [Internet]. Journal of Brazilian Chemical Society. 2005 ; 16( 6B): 1448-1453.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0103-50532005000800026
    • Vancouver

      Furtado NAJC, Pupo MT, Carvalho I, Campo VL, Duarte MCT, Bastos JK. Diketopiperazines produced by an Aspergillus fumigatus Brazilian strain [Internet]. Journal of Brazilian Chemical Society. 2005 ; 16( 6B): 1448-1453.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0103-50532005000800026
  • Fonte: Journal of Chemical Education. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      CARVALHO, Ivone e BORGES, Áurea Donizete Lanchote e BERNARDES, Lílian Sibelle Campos. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education, v. 82, n. 4, p. 588-596, 2005Tradução . . Acesso em: 18 nov. 2024.
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      Carvalho, I., Borges, Á. D. L., & Bernardes, L. S. C. (2005). Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education, 82( 4), 588-596.
    • NLM

      Carvalho I, Borges ÁDL, Bernardes LSC. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education. 2005 ; 82( 4): 588-596.[citado 2024 nov. 18 ]
    • Vancouver

      Carvalho I, Borges ÁDL, Bernardes LSC. Medicinal chemistry and molecular modeling:: An integration to teach drug structure-activity relationship and the molecular basis of drug action. Journal of Chemical Education. 2005 ; 82( 4): 588-596.[citado 2024 nov. 18 ]
  • Fonte: Journal of Computer-Aided Molecular Design. Unidade: FCFRP

    Assunto: SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA (TRATAMENTO)

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      TOMICH, C. H. et al. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors. Journal of Computer-Aided Molecular Design, v. 19, p. 83-92, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10822-005-1486-6. Acesso em: 18 nov. 2024.
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      Tomich, C. H., Silva, P. da, Carvalho, I., & Taft, C. A. (2005). Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors. Journal of Computer-Aided Molecular Design, 19, 83-92. doi:10.1007/s10822-005-1486-6
    • NLM

      Tomich CH, Silva P da, Carvalho I, Taft CA. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors [Internet]. Journal of Computer-Aided Molecular Design. 2005 ; 19 83-92.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10822-005-1486-6
    • Vancouver

      Tomich CH, Silva P da, Carvalho I, Taft CA. Homology modeling and molecular interaction field studies of 'alfa'-glucosidases as a guide to structure-based design of novel proposed anti-HIV inhibitors [Internet]. Journal of Computer-Aided Molecular Design. 2005 ; 19 83-92.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s10822-005-1486-6
  • Fonte: Carbohydrate Research. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      CARVALHO, Ivone e MELO, Eduardo Borges de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose. Carbohydrate Research, v. 339, p. 361-365, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.carres.2003.10.010. Acesso em: 18 nov. 2024.
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      Carvalho, I., & Melo, E. B. de. (2004). Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose. Carbohydrate Research, 339, 361-365. doi:10.1016/j.carres.2003.10.010
    • NLM

      Carvalho I, Melo EB de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose [Internet]. Carbohydrate Research. 2004 ; 339 361-365.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.carres.2003.10.010
    • Vancouver

      Carvalho I, Melo EB de. Synthesis of (+)-(2R,3S,4R)-2,3,4-trihydroxycyclohehanone from D-glucose [Internet]. Carbohydrate Research. 2004 ; 339 361-365.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.carres.2003.10.010
  • Fonte: Carbohydrate Research. Unidade: FCFRP

    Assunto: QUÍMICA FARMACÊUTICA

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      CARVALHO, Ivone et al. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters. Carbohydrate Research, v. 338, n. 10, p. 1039-1043, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0008-6215(03)00071-5. Acesso em: 18 nov. 2024.
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      Carvalho, I., Scheuerl, S. L., Kartha, K. P. R., & Field, R. A. (2003). Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters. Carbohydrate Research, 338( 10), 1039-1043. doi:10.1016/s0008-6215(03)00071-5
    • NLM

      Carvalho I, Scheuerl SL, Kartha KPR, Field RA. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters [Internet]. Carbohydrate Research. 2003 ; 338( 10): 1039-1043.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0008-6215(03)00071-5
    • Vancouver

      Carvalho I, Scheuerl SL, Kartha KPR, Field RA. Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-'beta'-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters [Internet]. Carbohydrate Research. 2003 ; 338( 10): 1039-1043.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0008-6215(03)00071-5

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