Filtros : "IQ-QFL" "ANDRADE, LEANDRO HELGUEIRA DE" "IQSC" Removidos: "Oliveira, José Eduardo de" "ISOLANI, PAULO CELSO" Limpar

Filtros



Refine with date range


  • Source: Química Nova. Unidades: IQSC, IQ

    Subjects: EDUCAÇÃO, QUÍMICA

    Versão PublicadaAcesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      Química Nova. Química Nova. São Paulo: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://quimicanova.sbq.org.br/conteudo.asp?page=5. Acesso em: 09 jun. 2024. , 2024
    • APA

      Química Nova. (2024). Química Nova. Química Nova. São Paulo: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://quimicanova.sbq.org.br/conteudo.asp?page=5
    • NLM

      Química Nova [Internet]. Química Nova. 2024 ;[citado 2024 jun. 09 ] Available from: https://quimicanova.sbq.org.br/conteudo.asp?page=5
    • Vancouver

      Química Nova [Internet]. Química Nova. 2024 ;[citado 2024 jun. 09 ] Available from: https://quimicanova.sbq.org.br/conteudo.asp?page=5
  • Source: Current Organic Synthesis. Unidades: IQ, IQSC

    Assunto: SÍNTESE ORGÂNICA

    PrivadoAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      ANDRADE, Leandro Helgueira et al. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil. Current Organic Synthesis, v. 12, p. 696-713, 2015Tradução . . Disponível em: https://doi.org/10.2174/157017941206150828103404. Acesso em: 09 jun. 2024.
    • APA

      Andrade, L. H., Sousa, B. A., Ferreira , I. M., & Porto, A. L. M. (2015). Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil. Current Organic Synthesis, 12, 696-713. doi:10.2174/157017941206150828103404
    • NLM

      Andrade LH, Sousa BA, Ferreira IM, Porto ALM. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil [Internet]. Current Organic Synthesis. 2015 ; 12 696-713.[citado 2024 jun. 09 ] Available from: https://doi.org/10.2174/157017941206150828103404
    • Vancouver

      Andrade LH, Sousa BA, Ferreira IM, Porto ALM. Contributions on kinetic resolution by lipases on the development of organic synthesis in Brazil [Internet]. Current Organic Synthesis. 2015 ; 12 696-713.[citado 2024 jun. 09 ] Available from: https://doi.org/10.2174/157017941206150828103404
  • Source: Food Technology and Biotechnology. Unidades: IQ, IQSC

    Subjects: TECNOLOGIA DE ALIMENTOS, BIOTECNOLOGIA

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PIOVAN, Leandro et al. Demethylation of N,N-Dimethylbenzenamine and N,N,3-Trimethylbenzenamine by Whole Cells of Aspergillus terreus. Food Technology and Biotechnology, v. 49, n. 4, p. 460-464, 2011Tradução . . Disponível em: http://www.ftb.com.hr/49/FTB_49-4_460.pdf. Acesso em: 09 jun. 2024.
    • APA

      Piovan, L., Kagohara, E., Vale, J. A., Comasseto, J. V., Shoenlein-Crusius, I. H., Andrade, L. H., & Porto, A. L. M. (2011). Demethylation of N,N-Dimethylbenzenamine and N,N,3-Trimethylbenzenamine by Whole Cells of Aspergillus terreus. Food Technology and Biotechnology, 49( 4), 460-464. Recuperado de http://www.ftb.com.hr/49/FTB_49-4_460.pdf
    • NLM

      Piovan L, Kagohara E, Vale JA, Comasseto JV, Shoenlein-Crusius IH, Andrade LH, Porto ALM. Demethylation of N,N-Dimethylbenzenamine and N,N,3-Trimethylbenzenamine by Whole Cells of Aspergillus terreus [Internet]. Food Technology and Biotechnology. 2011 ; 49( 4): 460-464.[citado 2024 jun. 09 ] Available from: http://www.ftb.com.hr/49/FTB_49-4_460.pdf
    • Vancouver

      Piovan L, Kagohara E, Vale JA, Comasseto JV, Shoenlein-Crusius IH, Andrade LH, Porto ALM. Demethylation of N,N-Dimethylbenzenamine and N,N,3-Trimethylbenzenamine by Whole Cells of Aspergillus terreus [Internet]. Food Technology and Biotechnology. 2011 ; 49( 4): 460-464.[citado 2024 jun. 09 ] Available from: http://www.ftb.com.hr/49/FTB_49-4_460.pdf
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: QUÍMICA, CÉLULAS

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PIOVAN, Leandro et al. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms. Tetrahedron - Asymmetry, v. 19, n. 20, p. 2385-2389, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.10.003. Acesso em: 09 jun. 2024.
    • APA

      Piovan, L., Kagohara, E., Ricci, L. C., Keppler, A. F., Capelari, M., Andrade, L. H., et al. (2008). Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms. Tetrahedron - Asymmetry, 19( 20), 2385-2389. doi:10.1016/j.tetasy.2008.10.003
    • NLM

      Piovan L, Kagohara E, Ricci LC, Keppler AF, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms [Internet]. Tetrahedron - Asymmetry. 2008 ; 19( 20): 2385-2389.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2008.10.003
    • Vancouver

      Piovan L, Kagohara E, Ricci LC, Keppler AF, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Chemoselective screening for the reduction of a chiral functionalised (+/-)-2-(phenylthio)cyclohexanone by whole cells of brazilian micro-organisms [Internet]. Tetrahedron - Asymmetry. 2008 ; 19( 20): 2385-2389.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2008.10.003
  • Source: Food Technology and Biotechnology. Unidades: IQ, IQSC

    Subjects: BACTÉRIAS, BIOTRANSFORMAÇÃO, QUÍMICA

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      KAGOHARA, Edna et al. Biotransformations of substituted phenylethanols and acetophenones by environmental bacteria. Food Technology and Biotechnology, v. 46 n. 4, p. 381-387, 2008Tradução . . Disponível em: http://www.ftb.com.hr/46-381.pdf. Acesso em: 09 jun. 2024.
    • APA

      Kagohara, E., Pellizari, V. H., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2008). Biotransformations of substituted phenylethanols and acetophenones by environmental bacteria. Food Technology and Biotechnology, 46 n. 4, 381-387. Recuperado de http://www.ftb.com.hr/46-381.pdf
    • NLM

      Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of substituted phenylethanols and acetophenones by environmental bacteria [Internet]. Food Technology and Biotechnology. 2008 ; 46 n. 4 381-387.[citado 2024 jun. 09 ] Available from: http://www.ftb.com.hr/46-381.pdf
    • Vancouver

      Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of substituted phenylethanols and acetophenones by environmental bacteria [Internet]. Food Technology and Biotechnology. 2008 ; 46 n. 4 381-387.[citado 2024 jun. 09 ] Available from: http://www.ftb.com.hr/46-381.pdf
  • Source: Química Nova. Unidades: IQ, IQSC

    Assunto: QUÍMICA

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      FERRAZ, Helena Maria Carvalho et al. Bioreduction of substituted a-tetralones promoted by Daucus carota root. Química Nova, v. 31, n. 4, p. 813-817, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-40422008000400020. Acesso em: 09 jun. 2024.
    • APA

      Ferraz, H. M. C., Bianco, G. G., Bombonato, F. I., Andrade, L. H., & Porto, A. L. M. (2008). Bioreduction of substituted a-tetralones promoted by Daucus carota root. Química Nova, 31( 4), 813-817. doi:10.1590/s0100-40422008000400020
    • NLM

      Ferraz HMC, Bianco GG, Bombonato FI, Andrade LH, Porto ALM. Bioreduction of substituted a-tetralones promoted by Daucus carota root [Internet]. Química Nova. 2008 ; 31( 4): 813-817.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1590/s0100-40422008000400020
    • Vancouver

      Ferraz HMC, Bianco GG, Bombonato FI, Andrade LH, Porto ALM. Bioreduction of substituted a-tetralones promoted by Daucus carota root [Internet]. Química Nova. 2008 ; 31( 4): 813-817.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1590/s0100-40422008000400020
  • Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química. Unidades: IQSC, IQ

    Assunto: QUÍMICA ORGÂNICA

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PIOVAN, Leandro et al. Redução de cicloalcanonas a-seleniladas e a-sulfeniladas por tramestes rigida CCB 285. 2007, Anais.. São Paulo: SBQ, 2007. . Acesso em: 09 jun. 2024.
    • APA

      Piovan, L., Porto, A. L. M., Capelari, M., Comasseto, J. V., & Andrade, L. H. (2007). Redução de cicloalcanonas a-seleniladas e a-sulfeniladas por tramestes rigida CCB 285. In Resumos. São Paulo: SBQ.
    • NLM

      Piovan L, Porto ALM, Capelari M, Comasseto JV, Andrade LH. Redução de cicloalcanonas a-seleniladas e a-sulfeniladas por tramestes rigida CCB 285. Resumos. 2007 ;[citado 2024 jun. 09 ]
    • Vancouver

      Piovan L, Porto ALM, Capelari M, Comasseto JV, Andrade LH. Redução de cicloalcanonas a-seleniladas e a-sulfeniladas por tramestes rigida CCB 285. Resumos. 2007 ;[citado 2024 jun. 09 ]
  • Source: Enzyme and Microbial Technology. Unidades: ICB, IQ, IQSC

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      RAMINELLI, Cristiano et al. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, v. 40, n. 2, p. 362-369, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2006.06.002. Acesso em: 09 jun. 2024.
    • APA

      Raminelli, C., Kagohara, E., Pellizari, V. H., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2007). Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, 40( 2), 362-369. doi:10.1016/j.enzmictec.2006.06.002
    • NLM

      Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
    • Vancouver

      Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, SÍNTESE ORGÂNICA, ASPERGILLUS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      OMORI, Álvaro Takeo et al. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1048-1053, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.04.019. Acesso em: 09 jun. 2024.
    • APA

      Omori, Á. T., Assis, L. F., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435. Tetrahedron - Asymmetry, 18( 9), 1048-1053. doi:10.1016/j.tetasy.2007.04.019
    • NLM

      Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
    • Vancouver

      Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, HIDROGENAÇÃO, LIPASE

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      FERRAZ, Helena Maria Carvalho et al. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry, v. 18, n. 9, p. 1070-1076, 2007Tradução . . Acesso em: 09 jun. 2024.
    • APA

      Ferraz, H. M. C., Bianco, G. G., Teixeira, C. C., Andrade, L. H., & Porto, A. L. M. (2007). Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry, 18( 9), 1070-1076.
    • NLM

      Ferraz HMC, Bianco GG, Teixeira CC, Andrade LH, Porto ALM. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1070-1076.[citado 2024 jun. 09 ]
    • Vancouver

      Ferraz HMC, Bianco GG, Teixeira CC, Andrade LH, Porto ALM. Enzymatic resolution of alpha-tetralols by CALB-catalyzed acetylation. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1070-1076.[citado 2024 jun. 09 ]
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: ANTIFÚNGICOS (ATIVIDADE), CANDIDA, PRODUTOS NATURAIS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      REIGADA, Juliana Beltrame et al. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 18, n. 9, p. 1054-1058, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.05.006. Acesso em: 09 jun. 2024.
    • APA

      Reigada, J. B., Tcacenco, C. M., Andrade, L. H., Kato, M. J., Porto, A. L. M., & Lago, J. H. G. (2007). Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 18( 9), 1054-1058. doi:10.1016/j.tetasy.2007.05.006
    • NLM

      Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
    • Vancouver

      Reigada JB, Tcacenco CM, Andrade LH, Kato MJ, Porto ALM, Lago JHG. Chemical constituents from Piper marginatum Jacq. (Piperaceae) - antifungal activities and kinetic resolution of (RS)-marginatumol by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1054-1058.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
  • Source: Enzyme and Microbial Technology. Unidades: IQ, ICB, IQSC

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PACHECO, Adriana de O. et al. Biotransformations of nitro-aromatic compounds to amines and acetamides by tuberous roots of Arracacia xanthorrhiza and Beta vulgaris and associated microorganism (Candida guilliermondii). Enzyme and Microbial Technology, v. 42, n. 1, p. 65-69, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2007.08.001. Acesso em: 09 jun. 2024.
    • APA

      Pacheco, A. de O., Kagohara, E., Andrade, L. H., Comasseto, J. V., Crusius, I. H. S., Paula, C. R., & Porto, A. L. M. (2007). Biotransformations of nitro-aromatic compounds to amines and acetamides by tuberous roots of Arracacia xanthorrhiza and Beta vulgaris and associated microorganism (Candida guilliermondii). Enzyme and Microbial Technology, 42( 1), 65-69. doi:10.1016/j.enzmictec.2007.08.001
    • NLM

      Pacheco A de O, Kagohara E, Andrade LH, Comasseto JV, Crusius IHS, Paula CR, Porto ALM. Biotransformations of nitro-aromatic compounds to amines and acetamides by tuberous roots of Arracacia xanthorrhiza and Beta vulgaris and associated microorganism (Candida guilliermondii) [Internet]. Enzyme and Microbial Technology. 2007 ; 42( 1): 65-69.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.enzmictec.2007.08.001
    • Vancouver

      Pacheco A de O, Kagohara E, Andrade LH, Comasseto JV, Crusius IHS, Paula CR, Porto ALM. Biotransformations of nitro-aromatic compounds to amines and acetamides by tuberous roots of Arracacia xanthorrhiza and Beta vulgaris and associated microorganism (Candida guilliermondii) [Internet]. Enzyme and Microbial Technology. 2007 ; 42( 1): 65-69.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.enzmictec.2007.08.001
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidades: IQ, IQSC

    Subjects: BIOTRANSFORMAÇÃO, ASPERGILLUS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      DA COSTA, Carlos Eduardo et al. Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus. Journal of Molecular Catalysis B - Enzymatic, v. 45, n. 3-4, p. 135-139, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.molcatb.2007.01.004. Acesso em: 09 jun. 2024.
    • APA

      Da Costa, C. E., Comasseto, J. V., Schoenlein-Crusius, I. H., Andrade, L. H., & Porto, A. L. M. (2007). Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus. Journal of Molecular Catalysis B - Enzymatic, 45( 3-4), 135-139. doi:10.1016/j.molcatb.2007.01.004
    • NLM

      Da Costa CE, Comasseto JV, Schoenlein-Crusius IH, Andrade LH, Porto ALM. Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2007 ; 45( 3-4): 135-139.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.molcatb.2007.01.004
    • Vancouver

      Da Costa CE, Comasseto JV, Schoenlein-Crusius IH, Andrade LH, Porto ALM. Biotransformation of 'beta'-hydroxyphenyl selenides, diphenyldiselenide and benzeneseleninic acid by whole cells of Aspergillus terreus [Internet]. Journal of Molecular Catalysis B - Enzymatic. 2007 ; 45( 3-4): 135-139.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.molcatb.2007.01.004
  • Source: Food Technology and Biotechnology. Unidades: IQ, IQSC

    Assunto: QUÍMICA

    Acesso à fonteHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      ASSIS, Leonardo Fernandes et al. Deracemization of (RS)-1-[(4-Methylselanyl)Phenyl]Ethanol and (RS)-1-[(4-Ethylselanyl)Phenyl]Ethanol by Strains of Aspergillus terreus. Food Technology and Biotechnology, v. 45, n. 4, p. 415-419, 2007Tradução . . Disponível em: http://www.ftb.com.hr/45-415.pdf. Acesso em: 09 jun. 2024.
    • APA

      Assis, L. F., Kagohara, E., Omori, Á. T., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2007). Deracemization of (RS)-1-[(4-Methylselanyl)Phenyl]Ethanol and (RS)-1-[(4-Ethylselanyl)Phenyl]Ethanol by Strains of Aspergillus terreus. Food Technology and Biotechnology, 45( 4), 415-419. Recuperado de http://www.ftb.com.hr/45-415.pdf
    • NLM

      Assis LF, Kagohara E, Omori ÁT, Comasseto JV, Andrade LH, Porto ALM. Deracemization of (RS)-1-[(4-Methylselanyl)Phenyl]Ethanol and (RS)-1-[(4-Ethylselanyl)Phenyl]Ethanol by Strains of Aspergillus terreus [Internet]. Food Technology and Biotechnology. 2007 ; 45( 4): 415-419.[citado 2024 jun. 09 ] Available from: http://www.ftb.com.hr/45-415.pdf
    • Vancouver

      Assis LF, Kagohara E, Omori ÁT, Comasseto JV, Andrade LH, Porto ALM. Deracemization of (RS)-1-[(4-Methylselanyl)Phenyl]Ethanol and (RS)-1-[(4-Ethylselanyl)Phenyl]Ethanol by Strains of Aspergillus terreus [Internet]. Food Technology and Biotechnology. 2007 ; 45( 4): 415-419.[citado 2024 jun. 09 ] Available from: http://www.ftb.com.hr/45-415.pdf
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: BOTÂNICA, QUÍMICA

    Acesso à fonteAcesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      PIOVAN, Leandro et al. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes. Tetrahedron - Asymmetry, v. 18, n. 12, p. 1398-1402, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2007.05.036. Acesso em: 09 jun. 2024.
    • APA

      Piovan, L., Capelari, M., Andrade, L. H., Comasseto, J. V., & Porto, A. L. M. (2007). Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes. Tetrahedron - Asymmetry, 18( 12), 1398-1402. doi:10.1016/j.tetasy.2007.05.036
    • NLM

      Piovan L, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 12): 1398-1402.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
    • Vancouver

      Piovan L, Capelari M, Andrade LH, Comasseto JV, Porto ALM. Biocatalytic reduction of a racemic selenocylohexanone by brazilian basidiomycetes [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 12): 1398-1402.[citado 2024 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      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: 09 jun. 2024.
    • APA

      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 jun. 09 ] 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 jun. 09 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014

Digital Library of Intellectual Production of Universidade de São Paulo     2012 - 2024