Filtros : "Indexado no Chemical Abstracts" "Andrade, Leandro Helgueira" "COMASSETO, JOAO VALDIR" Removidos: "FM-MPT" "Reino Unido" "Financiado pela FAPDF" Limpar

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  • Source: Enzyme and Microbial Technology. Unidades: ICB, IQ, IQSC

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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    • 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: 11 out. 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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, SÍNTESE ORGÂNICA, ASPERGILLUS

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    • 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: 11 out. 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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: Enzyme and Microbial Technology. Unidades: IQ, ICB, IQSC

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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    • 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: 11 out. 2024.
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      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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1016/j.enzmictec.2007.08.001
  • Source: Tetrahedron. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA

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    • ABNT

      RAMINELLI, Cristiano et al. Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes. Tetrahedron, v. 61, n. 2, p. 409-415, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2004.10.087. Acesso em: 11 out. 2024.
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      Raminelli, C., Silva, N. C. da, Dos Santos, A. A., Porto, A. L. M., Andrade, L. H., & Comasseto, J. V. (2005). Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes. Tetrahedron, 61( 2), 409-415. doi:10.1016/j.tet.2004.10.087
    • NLM

      Raminelli C, Silva NC da, Dos Santos AA, Porto ALM, Andrade LH, Comasseto JV. Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes [Internet]. Tetrahedron. 2005 ; 61( 2): 409-415.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tet.2004.10.087
    • Vancouver

      Raminelli C, Silva NC da, Dos Santos AA, Porto ALM, Andrade LH, Comasseto JV. Regio- and stereoselective synthesis of Z-vinylic tellurides from propargylic alcohols: a route to chiral Z-enynes [Internet]. Tetrahedron. 2005 ; 61( 2): 409-415.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tet.2004.10.087
  • Source: Enzyme and Microbial Technology. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, ASPERGILLUS, BIOTRANSFORMAÇÃO

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    • ABNT

      KEPPLER, Artur Franz et al. Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones. Enzyme and Microbial Technology, v. 36, n. 7, p. 967-975, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2005.01.024. Acesso em: 11 out. 2024.
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      Keppler, A. F., Porto, A. L. M., Schoenlein-Crusius, I. H., Comasseto, J. V., & Andrade, L. H. (2005). Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones. Enzyme and Microbial Technology, 36( 7), 967-975. doi:10.1016/j.enzmictec.2005.01.024
    • NLM

      Keppler AF, Porto ALM, Schoenlein-Crusius IH, Comasseto JV, Andrade LH. Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones [Internet]. Enzyme and Microbial Technology. 2005 ; 36( 7): 967-975.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.enzmictec.2005.01.024
    • Vancouver

      Keppler AF, Porto ALM, Schoenlein-Crusius IH, Comasseto JV, Andrade LH. Enzymatic evaluation of different Aspergillus strains by biotransformation of cyclic ketones [Internet]. Enzyme and Microbial Technology. 2005 ; 36( 7): 967-975.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.enzmictec.2005.01.024
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: QUÍMICA FINA, CANDIDA, LIPASE

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    • ABNT

      RAMINELLI, Cristiano et al. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435). Tetrahedron - Asymmetry, v. 15, n. 19, p. 3117-3122, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2004.08.022. Acesso em: 11 out. 2024.
    • APA

      Raminelli, C., Comasseto, J. V., Andrade, L. H., & Porto, A. L. M. (2004). Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435). Tetrahedron - Asymmetry, 15( 19), 3117-3122. doi:10.1016/j.tetasy.2004.08.022
    • NLM

      Raminelli C, Comasseto JV, Andrade LH, Porto ALM. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435) [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 19): 3117-3122.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tetasy.2004.08.022
    • Vancouver

      Raminelli C, Comasseto JV, Andrade LH, Porto ALM. Kinetic resolution of propargylic and allylic alcohols by Candida antarctica lipase (Novozyme 435) [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 19): 3117-3122.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tetasy.2004.08.022
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAGENTES ORGÂNICOS

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    • ABNT

      COMASSETO, João Valdir et al. Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root. Tetrahedron Letters, v. 45, n. 23, p. 473-476, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2003.11.011. Acesso em: 11 out. 2024.
    • APA

      Comasseto, J. V., Omori, Á. T., Porto, A. L. M., & Andrade, L. H. (2004). Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root. Tetrahedron Letters, 45( 23), 473-476. doi:10.1016/j.tetlet.2003.11.011
    • NLM

      Comasseto JV, Omori ÁT, Porto ALM, Andrade LH. Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root [Internet]. Tetrahedron Letters. 2004 ; 45( 23): 473-476.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2003.11.011
    • Vancouver

      Comasseto JV, Omori ÁT, Porto ALM, Andrade LH. Preparation of chiral organochalcogeno-alpha-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root [Internet]. Tetrahedron Letters. 2004 ; 45( 23): 473-476.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2003.11.011
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: ASPERGILLUS, ASSIMETRIA (REDUÇÃO), QUÍMICA ORGÂNICA

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      COMASSETO, João Valdir et al. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae. Tetrahedron - Asymmetry, v. 14, n. 6, p. 711-715, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0957-4166(03)00096-x. Acesso em: 11 out. 2024.
    • APA

      Comasseto, J. V., Omori, Á. T., Andrade, L. H., & Porto, A. L. M. (2003). Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae. Tetrahedron - Asymmetry, 14( 6), 711-715. doi:10.1016/s0957-4166(03)00096-x
    • NLM

      Comasseto JV, Omori ÁT, Andrade LH, Porto ALM. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae [Internet]. Tetrahedron - Asymmetry. 2003 ; 14( 6): 711-715.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/s0957-4166(03)00096-x
    • Vancouver

      Comasseto JV, Omori ÁT, Andrade LH, Porto ALM. Bioreduction of fluoroacetophenones by the fungi Aspergillus terreus and Rhizopus oryzae [Internet]. Tetrahedron - Asymmetry. 2003 ; 14( 6): 711-715.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/s0957-4166(03)00096-x

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