Filtros : "Indexado no Chemical Abstracts" "Donate, Paulo Marcos" Removidos: " FCF002" "HIST DA ARQ E ESTETICA DO PROJETO" "FISIOLOGIA" "Mendonça, Cleber Renato" "Ticianelli, Edson Antonio" Limpar

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  • Source: Journal of Molecular Structure. Unidades: FCFRP, FFCLRP

    Subjects: ESTEREOQUÍMICA, RESSONÂNCIA MAGNÉTICA NUCLEAR, QUÍMICA MÉDICA

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      PREVIDI, Daniel et al. Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations. Journal of Molecular Structure, v. 1178, p. 467-478, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2018.10.064. Acesso em: 03 jul. 2024.
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      Previdi, D., Nardini, V., Celorio, M. E. R., Palaretti, V., Silva, G. V. J. da, & Donate, P. M. (2019). Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations. Journal of Molecular Structure, 1178, 467-478. doi:10.1016/j.molstruc.2018.10.064
    • NLM

      Previdi D, Nardini V, Celorio MER, Palaretti V, Silva GVJ da, Donate PM. Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations [Internet]. Journal of Molecular Structure. 2019 ;1178 467-478.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.molstruc.2018.10.064
    • Vancouver

      Previdi D, Nardini V, Celorio MER, Palaretti V, Silva GVJ da, Donate PM. Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations [Internet]. Journal of Molecular Structure. 2019 ;1178 467-478.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.molstruc.2018.10.064
  • Source: Synthetic Communications. Unidade: FFCLRP

    Subjects: PRODUTOS NATURAIS (SÍNTESE QUÍMICA), SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      LAZARO, Aline S et al. New approach to the synthesis of the natural product aripuanin. Synthetic Communications, v. 45, n. 11, p. 1374-1378, 2015Tradução . . Disponível em: https://doi.org/10.1080/00397911.2015.1021426. Acesso em: 03 jul. 2024.
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      Lazaro, A. S., Ribeiro, P. H. Z., Sairre, M. I., & Donate, P. M. (2015). New approach to the synthesis of the natural product aripuanin. Synthetic Communications, 45( 11), 1374-1378. doi:10.1080/00397911.2015.1021426
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      Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1080/00397911.2015.1021426
    • Vancouver

      Lazaro AS, Ribeiro PHZ, Sairre MI, Donate PM. New approach to the synthesis of the natural product aripuanin [Internet]. Synthetic Communications. 2015 ; 45( 11): 1374-1378.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1080/00397911.2015.1021426
  • Source: Magnetic Resonance in Chemistry. Unidade: FFCLRP

    Subjects: PRODUTOS NATURAIS, LIGNINA

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      SILVA, Rosangela da et al. Complete assignments of 'ANTPOT.1 H' and 'ANTPOT. 13'C NMR spectral data for 7,7'- dihydroarylnaphthalene lignan lactones. Magnetic Resonance in Chemistry, v. 47, n. 6, p. 523-526, 2009Tradução . . Acesso em: 03 jul. 2024.
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      Silva, R. da, Batista, J. L. C., Maringolo, C. da S., & Donate, P. M. (2009). Complete assignments of 'ANTPOT.1 H' and 'ANTPOT. 13'C NMR spectral data for 7,7'- dihydroarylnaphthalene lignan lactones. Magnetic Resonance in Chemistry, 47( 6), 523-526.
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      Silva R da, Batista JLC, Maringolo C da S, Donate PM. Complete assignments of 'ANTPOT.1 H' and 'ANTPOT. 13'C NMR spectral data for 7,7'- dihydroarylnaphthalene lignan lactones. Magnetic Resonance in Chemistry. 2009 ; 47( 6): 523-526.[citado 2024 jul. 03 ]
    • Vancouver

      Silva R da, Batista JLC, Maringolo C da S, Donate PM. Complete assignments of 'ANTPOT.1 H' and 'ANTPOT. 13'C NMR spectral data for 7,7'- dihydroarylnaphthalene lignan lactones. Magnetic Resonance in Chemistry. 2009 ; 47( 6): 523-526.[citado 2024 jul. 03 ]
  • Source: Journal of the Brazilian Chemical Society. Unidade: FFCLRP

    Subjects: ANTIOXIDANTES, VITAMINA A

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      FREDERICO, Daniel e CONSTANTINO, Maurício Gomes e DONATE, Paulo Marcos. Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin. Journal of the Brazilian Chemical Society, v. 20, n. 5, p. 888-894, 2009Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532009000500013. Acesso em: 03 jul. 2024.
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      Frederico, D., Constantino, M. G., & Donate, P. M. (2009). Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin. Journal of the Brazilian Chemical Society, 20( 5), 888-894. doi:10.1590/s0103-50532009000500013
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      Frederico D, Constantino MG, Donate PM. Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 5): 888-894.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1590/s0103-50532009000500013
    • Vancouver

      Frederico D, Constantino MG, Donate PM. Total synthesis of (3S, 5R, 3'S, 5'S)-capsorubin [Internet]. Journal of the Brazilian Chemical Society. 2009 ; 20( 5): 888-894.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1590/s0103-50532009000500013
  • Source: Journal of The Brazilian Chemical Society. Unidade: FFCLRP

    Subjects: PLANTAS MEDICINAIS, BIOQUÍMICA

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      SAIRRE, Mirela Inês de et al. Synthesis and stereochemical assignment of methyl 3-(3-hydroxyphenoxy)acrylate via cis-trans photoisomerization. Journal of The Brazilian Chemical Society, v. 19, n. 1, p. 194-198, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532008000100027. Acesso em: 03 jul. 2024.
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      Sairre, M. I. de, Araújo, L. F. N., Silva, R. da, Donate, P. M., Silvério, C. A., & Okano, L. T. (2008). Synthesis and stereochemical assignment of methyl 3-(3-hydroxyphenoxy)acrylate via cis-trans photoisomerization. Journal of The Brazilian Chemical Society, 19( 1), 194-198. doi:10.1590/s0103-50532008000100027
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      Sairre MI de, Araújo LFN, Silva R da, Donate PM, Silvério CA, Okano LT. Synthesis and stereochemical assignment of methyl 3-(3-hydroxyphenoxy)acrylate via cis-trans photoisomerization [Internet]. Journal of The Brazilian Chemical Society. 2008 ; 19( 1): 194-198.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1590/s0103-50532008000100027
    • Vancouver

      Sairre MI de, Araújo LFN, Silva R da, Donate PM, Silvério CA, Okano LT. Synthesis and stereochemical assignment of methyl 3-(3-hydroxyphenoxy)acrylate via cis-trans photoisomerization [Internet]. Journal of The Brazilian Chemical Society. 2008 ; 19( 1): 194-198.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1590/s0103-50532008000100027
  • Source: Journal of Physical Chemistry. Part A. Unidades: FFCLRP, FCFRP

    Assunto: FÍSICO-QUÍMICA

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      KIRALJ, Rudolf et al. Conformational study of (8'alfa', 8'beta')-Bis(substituted phenyl)-lignano-9, 9'-lactones by means of combined computational, database mining, NMR, and chemometric approaches. Journal of Physical Chemistry. Part A, v. 111, n. 28, p. 6316-6333, 2007Tradução . . Acesso em: 03 jul. 2024.
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      Kiralj, R., Ferreira, M. M. C., Donate, P. M., Silva, R. da, & Albuquerque, S. de. (2007). Conformational study of (8'alfa', 8'beta')-Bis(substituted phenyl)-lignano-9, 9'-lactones by means of combined computational, database mining, NMR, and chemometric approaches. Journal of Physical Chemistry. Part A, 111( 28), 6316-6333.
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      Kiralj R, Ferreira MMC, Donate PM, Silva R da, Albuquerque S de. Conformational study of (8'alfa', 8'beta')-Bis(substituted phenyl)-lignano-9, 9'-lactones by means of combined computational, database mining, NMR, and chemometric approaches. Journal of Physical Chemistry. Part A. 2007 ; 111( 28): 6316-6333.[citado 2024 jul. 03 ]
    • Vancouver

      Kiralj R, Ferreira MMC, Donate PM, Silva R da, Albuquerque S de. Conformational study of (8'alfa', 8'beta')-Bis(substituted phenyl)-lignano-9, 9'-lactones by means of combined computational, database mining, NMR, and chemometric approaches. Journal of Physical Chemistry. Part A. 2007 ; 111( 28): 6316-6333.[citado 2024 jul. 03 ]
  • Source: Journal of Molecular Structure. Unidade: FFCLRP

    Assunto: ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)

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      SAIRRE, Mirela I. et al. Conformational influence on intramolecular cyclization for a 'beta'-ketoester containing oxirane ring: a theoretical and experimental study. Journal of Molecular Structure, v. 794, n. 1-3, p. 221-224, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2006.02.017. Acesso em: 03 jul. 2024.
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      Sairre, M. I., Bronze-Uhle, E. S., Donate, P. M., & Tormena, C. F. (2006). Conformational influence on intramolecular cyclization for a 'beta'-ketoester containing oxirane ring: a theoretical and experimental study. Journal of Molecular Structure, 794( 1-3), 221-224. doi:10.1016/j.molstruc.2006.02.017
    • NLM

      Sairre MI, Bronze-Uhle ES, Donate PM, Tormena CF. Conformational influence on intramolecular cyclization for a 'beta'-ketoester containing oxirane ring: a theoretical and experimental study [Internet]. Journal of Molecular Structure. 2006 ; 794( 1-3): 221-224.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.molstruc.2006.02.017
    • Vancouver

      Sairre MI, Bronze-Uhle ES, Donate PM, Tormena CF. Conformational influence on intramolecular cyclization for a 'beta'-ketoester containing oxirane ring: a theoretical and experimental study [Internet]. Journal of Molecular Structure. 2006 ; 794( 1-3): 221-224.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.molstruc.2006.02.017
  • Source: Journal of Molecular Catalysis A: Chemical. Unidade: FFCLRP

    Assunto: CATÁLISE

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      BRONZE-UHLE, Erika Soares et al. Enantioselective hydrogenation od 4-(hydroxymethyl) furan-2(5H)-one derivatives. Journal of Molecular Catalysis A: Chemical, v. 259, p. 103-107, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.molcata.2006.05.066. Acesso em: 03 jul. 2024.
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      Bronze-Uhle, E. S., Sairre, M. I. de, Donate, P. M., & Frederico, D. (2006). Enantioselective hydrogenation od 4-(hydroxymethyl) furan-2(5H)-one derivatives. Journal of Molecular Catalysis A: Chemical, 259, 103-107. doi:10.1016/j.molcata.2006.05.066
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      Bronze-Uhle ES, Sairre MI de, Donate PM, Frederico D. Enantioselective hydrogenation od 4-(hydroxymethyl) furan-2(5H)-one derivatives [Internet]. Journal of Molecular Catalysis A: Chemical. 2006 ; 259 103-107.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.molcata.2006.05.066
    • Vancouver

      Bronze-Uhle ES, Sairre MI de, Donate PM, Frederico D. Enantioselective hydrogenation od 4-(hydroxymethyl) furan-2(5H)-one derivatives [Internet]. Journal of Molecular Catalysis A: Chemical. 2006 ; 259 103-107.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.molcata.2006.05.066
  • Source: Journal of Physical Chemistry. Unidades: FFCLRP, FCFRP

    Assunto: FLAVONÓIDES (APLICAÇÕES TERAPÊUTICAS)

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      GUZZO, Mariana Rizzi et al. Study of the complexation of fisetin with cyclodextrins. Journal of Physical Chemistry, v. 110, p. 10545-10551, 2006Tradução . . Acesso em: 03 jul. 2024.
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      Guzzo, M. R., Uemi, M., Donate, P. M., Nikolaou, S., Machado, A. E. H., & Okano, L. T. (2006). Study of the complexation of fisetin with cyclodextrins. Journal of Physical Chemistry, 110, 10545-10551.
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      Guzzo MR, Uemi M, Donate PM, Nikolaou S, Machado AEH, Okano LT. Study of the complexation of fisetin with cyclodextrins. Journal of Physical Chemistry. 2006 ; 110 10545-10551.[citado 2024 jul. 03 ]
    • Vancouver

      Guzzo MR, Uemi M, Donate PM, Nikolaou S, Machado AEH, Okano LT. Study of the complexation of fisetin with cyclodextrins. Journal of Physical Chemistry. 2006 ; 110 10545-10551.[citado 2024 jul. 03 ]
  • Source: Spectrochimica Acta Part A. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

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      OLIVEIRA, Kleber Thiago de et al. Analysis of a cycloheptenone derivative: an experimental and theoretical approach. Spectrochimica Acta Part A, v. 63, p. 709-713, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2005.06.023. Acesso em: 03 jul. 2024.
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      Oliveira, K. T. de, Lacerda Júnior, V., Constantino, M. G., Donate, P. M., Silva, G. V. J. da, Brocksom, T. J., & Frederico, D. (2006). Analysis of a cycloheptenone derivative: an experimental and theoretical approach. Spectrochimica Acta Part A, 63, 709-713. doi:10.1016/j.saa.2005.06.023
    • NLM

      Oliveira KT de, Lacerda Júnior V, Constantino MG, Donate PM, Silva GVJ da, Brocksom TJ, Frederico D. Analysis of a cycloheptenone derivative: an experimental and theoretical approach [Internet]. Spectrochimica Acta Part A. 2006 ; 63 709-713.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.saa.2005.06.023
    • Vancouver

      Oliveira KT de, Lacerda Júnior V, Constantino MG, Donate PM, Silva GVJ da, Brocksom TJ, Frederico D. Analysis of a cycloheptenone derivative: an experimental and theoretical approach [Internet]. Spectrochimica Acta Part A. 2006 ; 63 709-713.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.saa.2005.06.023
  • Source: Spectrochimica Acta Part A. Unidades: FCFRP, FFCLRP

    Subjects: ANÁLISE ESPECTRAL, LIGANTES

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      HELENO, Vladimir Constantino Gomes et al. Detailed 'ANTIPOT.1H' and 'ANTIPOT.13C'NMR structural assignement of three biologically active lignan lactones. Spectrochimica Acta Part A, v. 63, p. 234-239, 2006Tradução . . Acesso em: 03 jul. 2024.
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      Heleno, V. C. G., Silva, R. da, Pedersoli, S., Albuquerque, S. de, Bastos, J. K., Silva, M. L. A. e, et al. (2006). Detailed 'ANTIPOT.1H' and 'ANTIPOT.13C'NMR structural assignement of three biologically active lignan lactones. Spectrochimica Acta Part A, 63, 234-239.
    • NLM

      Heleno VCG, Silva R da, Pedersoli S, Albuquerque S de, Bastos JK, Silva MLA e, Donate PM, Silva GVJ da, Lopes JLC. Detailed 'ANTIPOT.1H' and 'ANTIPOT.13C'NMR structural assignement of three biologically active lignan lactones. Spectrochimica Acta Part A. 2006 ; 63 234-239.[citado 2024 jul. 03 ]
    • Vancouver

      Heleno VCG, Silva R da, Pedersoli S, Albuquerque S de, Bastos JK, Silva MLA e, Donate PM, Silva GVJ da, Lopes JLC. Detailed 'ANTIPOT.1H' and 'ANTIPOT.13C'NMR structural assignement of three biologically active lignan lactones. Spectrochimica Acta Part A. 2006 ; 63 234-239.[citado 2024 jul. 03 ]
  • Source: Spectrochimica acta part A. Unidades: FCFRP, FFCLRP

    Subjects: FARMÁCIA, PRODUTOS NATURAIS

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      HELENO, Vladimir Constantino Gomes et al. Detailed 'H ANTPOT 1'and 'C ANTPOT 13'NMR structural assignment of three biologically active lignan lactones. Spectrochimica acta part A, v. 63, p. 234-239, 2005Tradução . . Acesso em: 03 jul. 2024.
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      Heleno, V. C. G., Silva, R. da, Pedersoli, S., Albuquerque, S. de, Bastos, J. K., Silva, M. L. A. e, et al. (2005). Detailed 'H ANTPOT 1'and 'C ANTPOT 13'NMR structural assignment of three biologically active lignan lactones. Spectrochimica acta part A, 63, 234-239.
    • NLM

      Heleno VCG, Silva R da, Pedersoli S, Albuquerque S de, Bastos JK, Silva MLA e, Donate PM, Silva GVJ da, Lopes JLC. Detailed 'H ANTPOT 1'and 'C ANTPOT 13'NMR structural assignment of three biologically active lignan lactones. Spectrochimica acta part A. 2005 ; 63 234-239.[citado 2024 jul. 03 ]
    • Vancouver

      Heleno VCG, Silva R da, Pedersoli S, Albuquerque S de, Bastos JK, Silva MLA e, Donate PM, Silva GVJ da, Lopes JLC. Detailed 'H ANTPOT 1'and 'C ANTPOT 13'NMR structural assignment of three biologically active lignan lactones. Spectrochimica acta part A. 2005 ; 63 234-239.[citado 2024 jul. 03 ]
  • Source: Journal of Brazilian Chemical Society. Unidade: FFCLRP

    Assunto: QUÍMICA ORGÂNICA

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      SILVA, Rosangela da et al. Racemic synthesis of 1,2-secomicrominutinin. Journal of Brazilian Chemical Society, v. 16, n. 3B, p. 626-633, 2005Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532005000400021. Acesso em: 03 jul. 2024.
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      Silva, R. da, Donate, P. M., Silva, G. V. J. da, Pedersoli, S., & Alemán, C. (2005). Racemic synthesis of 1,2-secomicrominutinin. Journal of Brazilian Chemical Society, 16( 3B), 626-633. doi:10.1590/s0103-50532005000400021
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      Silva R da, Donate PM, Silva GVJ da, Pedersoli S, Alemán C. Racemic synthesis of 1,2-secomicrominutinin [Internet]. Journal of Brazilian Chemical Society. 2005 ; 16( 3B): 626-633.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1590/s0103-50532005000400021
    • Vancouver

      Silva R da, Donate PM, Silva GVJ da, Pedersoli S, Alemán C. Racemic synthesis of 1,2-secomicrominutinin [Internet]. Journal of Brazilian Chemical Society. 2005 ; 16( 3B): 626-633.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1590/s0103-50532005000400021
  • Source: Tetrahedron Letters. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

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      SAIRRE, Mirela Inês e UHLE-BRONZE, Érika Soares e DONATE, Paulo Marcos. Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters. Tetrahedron Letters, v. 46, p. 2705-2708, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2005.01.158. Acesso em: 03 jul. 2024.
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      Sairre, M. I., Uhle-Bronze, É. S., & Donate, P. M. (2005). Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters. Tetrahedron Letters, 46, 2705-2708. doi:10.1016/j.tetlet.2005.01.158
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      Sairre MI, Uhle-Bronze ÉS, Donate PM. Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters [Internet]. Tetrahedron Letters. 2005 ; 46 2705-2708.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2005.01.158
    • Vancouver

      Sairre MI, Uhle-Bronze ÉS, Donate PM. Niobium(V) oxide: a new and efficient catalyst for the transesterification of 'beta-keto' esters [Internet]. Tetrahedron Letters. 2005 ; 46 2705-2708.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2005.01.158
  • Source: Magnetic Resonance in Chemistry. Unidades: FFCLRP, FCFRP

    Subjects: RESSONÂNCIA MAGNÉTICA (QUÍMICA), LIGNINA

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      SILVA, Rosangela da et al. Spectral assignments and reference data: complete assignments of '1 ANT POT H' and '13 AND POT C' NMR spectral data for benzylidenebenzyl butyrolactone lignans. Magnetic Resonance in Chemistry, v. 43, p. 966-969, 2005Tradução . . Acesso em: 03 jul. 2024.
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      Silva, R. da, Pedersoli, S., Lacerda Júnior, V., Donate, P. M., Albuquerque, S. de, Bastos, J. K., et al. (2005). Spectral assignments and reference data: complete assignments of '1 ANT POT H' and '13 AND POT C' NMR spectral data for benzylidenebenzyl butyrolactone lignans. Magnetic Resonance in Chemistry, 43, 966-969.
    • NLM

      Silva R da, Pedersoli S, Lacerda Júnior V, Donate PM, Albuquerque S de, Bastos JK, Araújo ALS de M, Silva MLA e. Spectral assignments and reference data: complete assignments of '1 ANT POT H' and '13 AND POT C' NMR spectral data for benzylidenebenzyl butyrolactone lignans. Magnetic Resonance in Chemistry. 2005 ; 43 966-969.[citado 2024 jul. 03 ]
    • Vancouver

      Silva R da, Pedersoli S, Lacerda Júnior V, Donate PM, Albuquerque S de, Bastos JK, Araújo ALS de M, Silva MLA e. Spectral assignments and reference data: complete assignments of '1 ANT POT H' and '13 AND POT C' NMR spectral data for benzylidenebenzyl butyrolactone lignans. Magnetic Resonance in Chemistry. 2005 ; 43 966-969.[citado 2024 jul. 03 ]
  • Source: Bollettino Chemico Farmaceutico. Unidades: FCFRP, FFCLRP

    Subjects: ANALGÉSICOS, ANTI-INFLAMATÓRIOS

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      COIMBRA, H. dos S. et al. Analgesic and anti-inflammatory activities of (-)-0 benzyl cubebin, a (-)-cubebin derivative, obtainned by partial synthesis. Bollettino Chemico Farmaceutico, v. 143, n. 2, p. 65-70, 2004Tradução . . Acesso em: 03 jul. 2024.
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      Coimbra, H. dos S., Royo, V. de A., Souza, V. A. de, Pereira, A. C., Souza, G. H. B., Silva, R. da, et al. (2004). Analgesic and anti-inflammatory activities of (-)-0 benzyl cubebin, a (-)-cubebin derivative, obtainned by partial synthesis. Bollettino Chemico Farmaceutico, 143( 2), 65-70.
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      Coimbra H dos S, Royo V de A, Souza VA de, Pereira AC, Souza GHB, Silva R da, Donate PM, Silva MLA, Cunha WR, Carvalho JCT, Bastos JK. Analgesic and anti-inflammatory activities of (-)-0 benzyl cubebin, a (-)-cubebin derivative, obtainned by partial synthesis. Bollettino Chemico Farmaceutico. 2004 ; 143( 2): 65-70.[citado 2024 jul. 03 ]
    • Vancouver

      Coimbra H dos S, Royo V de A, Souza VA de, Pereira AC, Souza GHB, Silva R da, Donate PM, Silva MLA, Cunha WR, Carvalho JCT, Bastos JK. Analgesic and anti-inflammatory activities of (-)-0 benzyl cubebin, a (-)-cubebin derivative, obtainned by partial synthesis. Bollettino Chemico Farmaceutico. 2004 ; 143( 2): 65-70.[citado 2024 jul. 03 ]
  • Source: Magnetic resonance in Chemistry. Unidades: FCFRP, FFCLRP

    Assunto: PRODUTOS NATURAIS

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      SILVA, Rosângela da et al. Complete assignment of H and c NMR data for three aryltetralin lignan lactones. Magnetic resonance in Chemistry, v. 42, p. 985-989, 2004Tradução . . Disponível em: https://doi.org/10.1002/mrc.1482. Acesso em: 03 jul. 2024.
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      Silva, R. da, Heleno, V. C. G., Albuquerque, S. de, Bastos, J. K., Andrade e Silva, M. L., Donate, P. M., & Silva, G. V. J. da. (2004). Complete assignment of H and c NMR data for three aryltetralin lignan lactones. Magnetic resonance in Chemistry, 42, 985-989. doi:10.1002/mrc.1482
    • NLM

      Silva R da, Heleno VCG, Albuquerque S de, Bastos JK, Andrade e Silva ML, Donate PM, Silva GVJ da. Complete assignment of H and c NMR data for three aryltetralin lignan lactones [Internet]. Magnetic resonance in Chemistry. 2004 ; 42 985-989.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/mrc.1482
    • Vancouver

      Silva R da, Heleno VCG, Albuquerque S de, Bastos JK, Andrade e Silva ML, Donate PM, Silva GVJ da. Complete assignment of H and c NMR data for three aryltetralin lignan lactones [Internet]. Magnetic resonance in Chemistry. 2004 ; 42 985-989.[citado 2024 jul. 03 ] Available from: https://doi.org/10.1002/mrc.1482
  • Source: Tetrahedron. Unidades: FFCLRP, FCFRP

    Assunto: FÁRMACOS (QUÍMICA)

    Acesso à fonteDOIHow to cite
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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: 03 jul. 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 jul. 03 ] 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 jul. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031
  • Source: Journal of Organie Chemistry. Unidade: FFCLRP

    Assunto: SÍNTESE ORGÂNICA

    How to cite
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    • ABNT

      FREDERICO, Daniel et al. A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry, v. 68, p. 9126-9128, 2003Tradução . . Acesso em: 03 jul. 2024.
    • APA

      Frederico, D., Donate, P. M., Constantino, M. G., Bronze, É. S., & Sairre, M. I. (2003). A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry, 68, 9126-9128.
    • NLM

      Frederico D, Donate PM, Constantino MG, Bronze ÉS, Sairre MI. A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry. 2003 ; 68 9126-9128.[citado 2024 jul. 03 ]
    • Vancouver

      Frederico D, Donate PM, Constantino MG, Bronze ÉS, Sairre MI. A short and efficient synthesis of crocetin-dimethylester and crocetindial. Journal of Organie Chemistry. 2003 ; 68 9126-9128.[citado 2024 jul. 03 ]
  • Source: Synthetic Communications. Unidade: FFCLRP

    Assunto: QUÍMICA

    How to cite
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    • ABNT

      DONATE, Paulo Marcos et al. Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications, v. 31, n. 1, p. 141-150, 2001Tradução . . Acesso em: 03 jul. 2024.
    • APA

      Donate, P. M., Silva, R. da, Silva, G. V. J. da, & Alemán, C. (2001). Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications, 31( 1), 141-150.
    • NLM

      Donate PM, Silva R da, Silva GVJ da, Alemán C. Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications. 2001 ; 31( 1): 141-150.[citado 2024 jul. 03 ]
    • Vancouver

      Donate PM, Silva R da, Silva GVJ da, Alemán C. Synthesis of benzofuranofuran derivatives: model of natural products. Synthetic Communications. 2001 ; 31( 1): 141-150.[citado 2024 jul. 03 ]

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