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  • Source: Journal of Photochemistry and Photobiology A: Chemistry. Unidade: IQ

    Subjects: VISCOSIDADE DO FLUXO DOS LÍQUIDOS, FOTOQUÍMICA, LUMINESCÊNCIA

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      KHALID, Muhammad et al. Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures. Journal of Photochemistry and Photobiology A: Chemistry, v. 312, p. 81-87, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jphotochem.2015.06.031. Acesso em: 04 set. 2024.
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      khalid, M., Oliveira, M. A. de, Souza Junior, S. P. de, Ciscato, L. F. M. L., Bartoloni, F. H., & Baader, W. J. (2015). Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures. Journal of Photochemistry and Photobiology A: Chemistry, 312, 81-87. doi:10.1016/j.jphotochem.2015.06.031
    • NLM

      khalid M, Oliveira MA de, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures [Internet]. Journal of Photochemistry and Photobiology A: Chemistry. 2015 ; 312 81-87.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.jphotochem.2015.06.031
    • Vancouver

      khalid M, Oliveira MA de, Souza Junior SP de, Ciscato LFML, Bartoloni FH, Baader WJ. Efficiency of intermolecular chemiluminescence systems lacks significant solvent cavity effect in binary toluene/diphenylmethane mixtures [Internet]. Journal of Photochemistry and Photobiology A: Chemistry. 2015 ; 312 81-87.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.jphotochem.2015.06.031
  • Source: Molecules. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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      SILVA, Siguara Bastos de Lemos e et al. Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine. Molecules, v. 20, n. 1, p. 1475-1494, 2015Tradução . . Disponível em: https://doi.org/10.3390/molecules20011475. Acesso em: 04 set. 2024.
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      Silva, S. B. de L. e, Della Torre, A., Carvalho, J. E. de, Ruiz, A. L. T. G. de, & Silva Junior, L. F. da. (2015). Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine. Molecules, 20( 1), 1475-1494. doi:10.3390/molecules20011475
    • NLM

      Silva SB de L e, Della Torre A, Carvalho JE de, Ruiz ALTG de, Silva Junior LF da. Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine [Internet]. Molecules. 2015 ; 20( 1): 1475-1494.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules20011475
    • Vancouver

      Silva SB de L e, Della Torre A, Carvalho JE de, Ruiz ALTG de, Silva Junior LF da. Seven-membered rings through metal-free rearrangement mediated by hypervalent iodine [Internet]. Molecules. 2015 ; 20( 1): 1475-1494.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules20011475
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: HIDROCARBONOS, SÍNTESE ORGÂNICA

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      BESORA, Maria et al. A computational view on the reactions of hydrocarbons with coinage metal complexes. Journal of Organometallic Chemistry, v. 784, p. 1-12, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2014.10.009. Acesso em: 04 set. 2024.
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      Besora, M., Braga, A. A. C., Sameera, W. M. C., Urbano, J., Fructos, M. R., Pérez, P. J., & Maseras, F. (2015). A computational view on the reactions of hydrocarbons with coinage metal complexes. Journal of Organometallic Chemistry, 784, 1-12. doi:10.1016/j.jorganchem.2014.10.009
    • NLM

      Besora M, Braga AAC, Sameera WMC, Urbano J, Fructos MR, Pérez PJ, Maseras F. A computational view on the reactions of hydrocarbons with coinage metal complexes [Internet]. Journal of Organometallic Chemistry. 2015 ; 784 1-12.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.jorganchem.2014.10.009
    • Vancouver

      Besora M, Braga AAC, Sameera WMC, Urbano J, Fructos MR, Pérez PJ, Maseras F. A computational view on the reactions of hydrocarbons with coinage metal complexes [Internet]. Journal of Organometallic Chemistry. 2015 ; 784 1-12.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.jorganchem.2014.10.009
  • Source: Materials. Unidade: IQ

    Subjects: COLÁGENO, POLÍMEROS SINTÉTICOS

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      GONÇALVES, Flavia et al. Hybrid membranes of PLLA/collagen for bone tissue engineering: a comparative study of Scaffold production techniques for optimal mechanical properties and osteoinduction ability. Materials, v. 8, n. 2, p. 408-423, 2015Tradução . . Disponível em: https://doi.org/10.3390/ma8020408. Acesso em: 04 set. 2024.
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      Gonçalves, F., Bentini, R., Burrows, M. C., Carreira, A. C. O., Kossugue, P. M., Sogayar, M. C., & Catalani, L. H. (2015). Hybrid membranes of PLLA/collagen for bone tissue engineering: a comparative study of Scaffold production techniques for optimal mechanical properties and osteoinduction ability. Materials, 8( 2), 408-423. doi:10.3390/ma8020408
    • NLM

      Gonçalves F, Bentini R, Burrows MC, Carreira ACO, Kossugue PM, Sogayar MC, Catalani LH. Hybrid membranes of PLLA/collagen for bone tissue engineering: a comparative study of Scaffold production techniques for optimal mechanical properties and osteoinduction ability [Internet]. Materials. 2015 ; 8( 2): 408-423.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/ma8020408
    • Vancouver

      Gonçalves F, Bentini R, Burrows MC, Carreira ACO, Kossugue PM, Sogayar MC, Catalani LH. Hybrid membranes of PLLA/collagen for bone tissue engineering: a comparative study of Scaffold production techniques for optimal mechanical properties and osteoinduction ability [Internet]. Materials. 2015 ; 8( 2): 408-423.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/ma8020408
  • Source: Molecules. Unidade: IQ

    Subjects: SCHISTOSOMA, CONTROLE DE VETORES

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      RAPADO, Ludmila Nakamura et al. A benzoic acid derivative and flavokawains from Piper species as Schistosomiasis vector controls. Molecules, v. 19, n. 4, p. 5205-5218, 2014Tradução . . Disponível em: https://doi.org/10.3390/molecules19045205. Acesso em: 04 set. 2024.
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      Rapado, L. N., Freitas, G. C., Polpo, A., Cardozo, M. R., Rincón, J. V., Scotti, M. T., et al. (2014). A benzoic acid derivative and flavokawains from Piper species as Schistosomiasis vector controls. Molecules, 19( 4), 5205-5218. doi:10.3390/molecules19045205
    • NLM

      Rapado LN, Freitas GC, Polpo A, Cardozo MR, Rincón JV, Scotti MT, Kato MJ, Nakano E, Yamaguchi LF. A benzoic acid derivative and flavokawains from Piper species as Schistosomiasis vector controls [Internet]. Molecules. 2014 ; 19( 4): 5205-5218.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules19045205
    • Vancouver

      Rapado LN, Freitas GC, Polpo A, Cardozo MR, Rincón JV, Scotti MT, Kato MJ, Nakano E, Yamaguchi LF. A benzoic acid derivative and flavokawains from Piper species as Schistosomiasis vector controls [Internet]. Molecules. 2014 ; 19( 4): 5205-5218.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules19045205
  • Source: Sensors and Actuators B. Unidade: IQ

    Subjects: POLÍMEROS (QUÍMICA ORGÂNICA), MATERIAIS COMPÓSITOS

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      ESTEVES, Carlos Henrique Alves et al. New composite porphyrin-conductive polymer gas sensors for application in electronic noses. Sensors and Actuators B, v. 193, p. 136-141, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.snb.2013.11.022. Acesso em: 04 set. 2024.
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      Esteves, C. H. A., Iglesias, B. A., Li, R. W. C., Ogawa, T., Araki, K., & Gruber, J. (2014). New composite porphyrin-conductive polymer gas sensors for application in electronic noses. Sensors and Actuators B, 193, 136-141. doi:10.1016/j.snb.2013.11.022
    • NLM

      Esteves CHA, Iglesias BA, Li RWC, Ogawa T, Araki K, Gruber J. New composite porphyrin-conductive polymer gas sensors for application in electronic noses [Internet]. Sensors and Actuators B. 2014 ; 193 136-141.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.snb.2013.11.022
    • Vancouver

      Esteves CHA, Iglesias BA, Li RWC, Ogawa T, Araki K, Gruber J. New composite porphyrin-conductive polymer gas sensors for application in electronic noses [Internet]. Sensors and Actuators B. 2014 ; 193 136-141.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.snb.2013.11.022
  • Source: Molecules. Unidade: IQ

    Subjects: ALDEÍDOS, SÍNTESE ORGÂNICA

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      REDDY, Kachi R. Kishore Kumar et al. Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes. Molecules, v. 18, n. 9, p. 11100-11130, 2013Tradução . . Disponível em: https://doi.org/10.3390/molecules180911100. Acesso em: 04 set. 2024.
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      Reddy, K. R. K. K., Rosa, I. M. L. R., Doriguetto, A. C., Bastos, E. L., & Silva Junior, L. F. da. (2013). Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes. Molecules, 18( 9), 11100-11130. doi:10.3390/molecules180911100
    • NLM

      Reddy KRKK, Rosa IMLR, Doriguetto AC, Bastos EL, Silva Junior LF da. Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes [Internet]. Molecules. 2013 ; 18( 9): 11100-11130.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules180911100
    • Vancouver

      Reddy KRKK, Rosa IMLR, Doriguetto AC, Bastos EL, Silva Junior LF da. Iodine-catalyzed prins cyclization of homoallylic alcohols and aldehydes [Internet]. Molecules. 2013 ; 18( 9): 11100-11130.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules180911100
  • Source: Chemoecology. Unidade: IQ

    Subjects: BIOTRANSFORMAÇÃO, COLEOPTERA

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      RAMOS, Clécio Sousa e KATO, Massuo Jorge. Metabolism of neolignans from P. regnellii (Piperaceae) in the beetle Naupactus bipes (Coleoptera: Curculionidae). Chemoecology, v. 23, n. 3, p. 143-148, 2013Tradução . . Disponível em: https://doi.org/10.1007/s00049-013-0129-y. Acesso em: 04 set. 2024.
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      Ramos, C. S., & Kato, M. J. (2013). Metabolism of neolignans from P. regnellii (Piperaceae) in the beetle Naupactus bipes (Coleoptera: Curculionidae). Chemoecology, 23( 3), 143-148. doi:10.1007/s00049-013-0129-y
    • NLM

      Ramos CS, Kato MJ. Metabolism of neolignans from P. regnellii (Piperaceae) in the beetle Naupactus bipes (Coleoptera: Curculionidae) [Internet]. Chemoecology. 2013 ; 23( 3): 143-148.[citado 2024 set. 04 ] Available from: https://doi.org/10.1007/s00049-013-0129-y
    • Vancouver

      Ramos CS, Kato MJ. Metabolism of neolignans from P. regnellii (Piperaceae) in the beetle Naupactus bipes (Coleoptera: Curculionidae) [Internet]. Chemoecology. 2013 ; 23( 3): 143-148.[citado 2024 set. 04 ] Available from: https://doi.org/10.1007/s00049-013-0129-y
  • Source: Molecules. Unidade: IQ

    Subjects: ESPECTROSCOPIA INFRAVERMELHA, DIFRAÇÃO POR RAIOS X

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      OLIVATO, Paulo Roberto et al. Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones. Molecules, v. 18, n. 7, p. 7492-7509, 2013Tradução . . Disponível em: https://doi.org/10.3390/molecules18077492. Acesso em: 04 set. 2024.
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      Olivato, P. R., Santos, J. M. M., Contieri, B., Cerqueira Júnior, C. R., Rodrigues, D. N. S., Vinhato, E., et al. (2013). Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones. Molecules, 18( 7), 7492-7509. doi:10.3390/molecules18077492
    • NLM

      Olivato PR, Santos JMM, Contieri B, Cerqueira Júnior CR, Rodrigues DNS, Vinhato E, Zukerman-Schpector J, Dal Colle M. Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones [Internet]. Molecules. 2013 ; 18( 7): 7492-7509.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules18077492
    • Vancouver

      Olivato PR, Santos JMM, Contieri B, Cerqueira Júnior CR, Rodrigues DNS, Vinhato E, Zukerman-Schpector J, Dal Colle M. Spectroscopic and Theoretical Studies of Some 3-(4′-Substituted phenylsulfanyl)-1-methyl-2-piperidones [Internet]. Molecules. 2013 ; 18( 7): 7492-7509.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules18077492
  • Source: Chemoecology. Unidade: IQ

    Assunto: BIOTRANSFORMAÇÃO

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      RAMOS, Clécio Sousa et al. Biotransformation of 4-nerolidylcatechol by Heraclides brasiliensis (Lepidoptera: Papilionidae) reduces the toxicity of Piper umbellata (Piperaceae). Chemoecology, v. 22, n. 1, p. 39-45, 2012Tradução . . Disponível em: https://doi.org/10.1007/s00049-011-0096-0. Acesso em: 04 set. 2024.
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      Ramos, C. S., Souza, L. de J., Kato, M. J., & Batista, R. (2012). Biotransformation of 4-nerolidylcatechol by Heraclides brasiliensis (Lepidoptera: Papilionidae) reduces the toxicity of Piper umbellata (Piperaceae). Chemoecology, 22( 1), 39-45. doi:10.1007/s00049-011-0096-0
    • NLM

      Ramos CS, Souza L de J, Kato MJ, Batista R. Biotransformation of 4-nerolidylcatechol by Heraclides brasiliensis (Lepidoptera: Papilionidae) reduces the toxicity of Piper umbellata (Piperaceae) [Internet]. Chemoecology. 2012 ; 22( 1): 39-45.[citado 2024 set. 04 ] Available from: https://doi.org/10.1007/s00049-011-0096-0
    • Vancouver

      Ramos CS, Souza L de J, Kato MJ, Batista R. Biotransformation of 4-nerolidylcatechol by Heraclides brasiliensis (Lepidoptera: Papilionidae) reduces the toxicity of Piper umbellata (Piperaceae) [Internet]. Chemoecology. 2012 ; 22( 1): 39-45.[citado 2024 set. 04 ] Available from: https://doi.org/10.1007/s00049-011-0096-0
  • Source: Molecules. Unidade: IQ

    Subjects: NEOPLASIAS, PRODUTOS NATURAIS

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      REDDY, Kachi R. Kishore Kumar et al. Populene D analogues: design, concise synthesis and antiproliferative activity. Molecules, v. 17, n. 8, p. 9621-9630, 2012Tradução . . Disponível em: https://doi.org/10.3390/molecules17089621. Acesso em: 04 set. 2024.
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      Reddy, K. R. K. K., Longato, G. B., Carvalho, J. E. de, Ruiz, A. L. T. G., & Silva Junior, L. F. da. (2012). Populene D analogues: design, concise synthesis and antiproliferative activity. Molecules, 17( 8), 9621-9630. doi:10.3390/molecules17089621
    • NLM

      Reddy KRKK, Longato GB, Carvalho JE de, Ruiz ALTG, Silva Junior LF da. Populene D analogues: design, concise synthesis and antiproliferative activity [Internet]. Molecules. 2012 ; 17( 8): 9621-9630.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules17089621
    • Vancouver

      Reddy KRKK, Longato GB, Carvalho JE de, Ruiz ALTG, Silva Junior LF da. Populene D analogues: design, concise synthesis and antiproliferative activity [Internet]. Molecules. 2012 ; 17( 8): 9621-9630.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules17089621
  • Source: Journal of Photochemistry and Photobiology A: Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, PEROXIDASE

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      CISCATO, Luiz Francisco Monteiro Leite et al. Fenchyl substituted 1,2-dioxetanes as an alternative to adamantyl derivatives for bioanalytical applications. Journal of Photochemistry and Photobiology A: Chemistry, v. 218, n. 1, p. 41-47, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.jphotochem.2010.12.001. Acesso em: 04 set. 2024.
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      Ciscato, L. F. M. L., Weiss, D., Beckert, R., & Baader, W. J. (2011). Fenchyl substituted 1,2-dioxetanes as an alternative to adamantyl derivatives for bioanalytical applications. Journal of Photochemistry and Photobiology A: Chemistry, 218( 1), 41-47. doi:10.1016/j.jphotochem.2010.12.001
    • NLM

      Ciscato LFML, Weiss D, Beckert R, Baader WJ. Fenchyl substituted 1,2-dioxetanes as an alternative to adamantyl derivatives for bioanalytical applications [Internet]. Journal of Photochemistry and Photobiology A: Chemistry. 2011 ; 218( 1): 41-47.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.jphotochem.2010.12.001
    • Vancouver

      Ciscato LFML, Weiss D, Beckert R, Baader WJ. Fenchyl substituted 1,2-dioxetanes as an alternative to adamantyl derivatives for bioanalytical applications [Internet]. Journal of Photochemistry and Photobiology A: Chemistry. 2011 ; 218( 1): 41-47.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.jphotochem.2010.12.001
  • Source: Materials Chemistry and Physics. Unidade: IQ

    Assunto: POLÍMEROS (QUÍMICA ORGÂNICA)

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      FREITAS, Jilian Nei de et al. Conjugated copolymers based on poly(fluorenylene vinylene) derivatives containing push-pull units: synthesis and characterization. Materials Chemistry and Physics, v. 130, n. 1-2, p. 223-230, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.matchemphys.2011.06.029. Acesso em: 04 set. 2024.
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      Freitas, J. N. de, Li, R. W. C., Nogueira, A. F., & Gruber, J. (2011). Conjugated copolymers based on poly(fluorenylene vinylene) derivatives containing push-pull units: synthesis and characterization. Materials Chemistry and Physics, 130( 1-2), 223-230. doi:10.1016/j.matchemphys.2011.06.029
    • NLM

      Freitas JN de, Li RWC, Nogueira AF, Gruber J. Conjugated copolymers based on poly(fluorenylene vinylene) derivatives containing push-pull units: synthesis and characterization [Internet]. Materials Chemistry and Physics. 2011 ; 130( 1-2): 223-230.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.matchemphys.2011.06.029
    • Vancouver

      Freitas JN de, Li RWC, Nogueira AF, Gruber J. Conjugated copolymers based on poly(fluorenylene vinylene) derivatives containing push-pull units: synthesis and characterization [Internet]. Materials Chemistry and Physics. 2011 ; 130( 1-2): 223-230.[citado 2024 set. 04 ] Available from: https://doi.org/10.1016/j.matchemphys.2011.06.029
  • Source: Molecules. Unidades: IP, IQ

    Subjects: DROGAS DE ABUSO, COCAÍNA

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      KAMEYAMA, Márcia et al. Indatraline: synthesis and effect on the motor activity of wistar rats. Molecules, v. 16, n. 11, p. 9421-9438, 2011Tradução . . Disponível em: https://doi.org/10.3390/molecules16119421. Acesso em: 04 set. 2024.
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      Kameyama, M., Siqueira, F. A. de, Mijares, M. G., Silva Junior, L. F. da, & Silva, M. T. de A. (2011). Indatraline: synthesis and effect on the motor activity of wistar rats. Molecules, 16( 11), 9421-9438. doi:10.3390/molecules16119421
    • NLM

      Kameyama M, Siqueira FA de, Mijares MG, Silva Junior LF da, Silva MT de A. Indatraline: synthesis and effect on the motor activity of wistar rats [Internet]. Molecules. 2011 ; 16( 11): 9421-9438.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules16119421
    • Vancouver

      Kameyama M, Siqueira FA de, Mijares MG, Silva Junior LF da, Silva MT de A. Indatraline: synthesis and effect on the motor activity of wistar rats [Internet]. Molecules. 2011 ; 16( 11): 9421-9438.[citado 2024 set. 04 ] Available from: https://doi.org/10.3390/molecules16119421

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