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  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: QUÍMICA, CÉLULAS

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    • 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: 03 jun. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2008.10.003
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: AMINAS (COMPOSTOS ORGÂNICOS), REAGENTES ORGÂNICOS

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    • ABNT

      ANDRADE, Leandro Helgueira e SILVA, Alexandre Vieira. First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, v. 19, n. 10, p. 1175-1181, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2008.04.026. Acesso em: 03 jun. 2024.
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      Andrade, L. H., & Silva, A. V. (2008). First chemoenzymatic synthesis of organoselenium amines and amides. Tetrahedron - Asymmetry, 19( 10), 1175-1181. doi:10.1016/j.tetasy.2008.04.026
    • NLM

      Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
    • Vancouver

      Andrade LH, Silva AV. First chemoenzymatic synthesis of organoselenium amines and amides [Internet]. Tetrahedron - Asymmetry. 2008 ;19( 10): 1175-1181.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2008.04.026
  • 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: 03 jun. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, HIDROGENAÇÃO, LIPASE

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    • 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: 03 jun. 2024.
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      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. 03 ]
    • 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. 03 ]
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: ANTIFÚNGICOS (ATIVIDADE), CANDIDA, PRODUTOS NATURAIS

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    • 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: 03 jun. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.006
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: BOTÂNICA, QUÍMICA

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    • 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: 03 jun. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: LIPASE, QUÍMICA ORGÂNICA

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    • ABNT

      DOS SANTOS, Alcindo Aparecido et al. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, v. 17, n. 15, p. 2252-2259, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.024. Acesso em: 03 jun. 2024.
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      Dos Santos, A. A., Da Costa, C. E., Princival, J. L., & Comasseto, J. V. (2006). Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, 17( 15), 2252-2259. doi:10.1016/j.tetasy.2006.07.024
    • NLM

      Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
    • Vancouver

      Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, QUÍMICA ORGÂNICA

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      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: 03 jun. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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      GARIANI, Rogério Aparecido et al. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination. Tetrahedron - Asymmetry, v. 17, n. 20, p. 2930-2934, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.10.034. Acesso em: 03 jun. 2024.
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      Gariani, R. A., Simonelli, F., Oliveira, A. R. M. de, Barison, A., & Comasseto, J. V. (2006). A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination. Tetrahedron - Asymmetry, 17( 20), 2930-2934. doi:10.1016/j.tetasy.2006.10.034
    • NLM

      Gariani RA, Simonelli F, Oliveira ARM de, Barison A, Comasseto JV. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 20): 2930-2934.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2006.10.034
    • Vancouver

      Gariani RA, Simonelli F, Oliveira ARM de, Barison A, Comasseto JV. A chiral tellurium ferrocene as a chiral agent in NMR enantiomeric purity determination [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 20): 2930-2934.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2006.10.034
  • Source: Tetrahedron - Asymmetry. Unidade: FZEA

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      LUNARDI, Inês et al. Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum. Tetrahedron - Asymmetry, v. 16, n. 15, p. 2515-2519, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2005.06.020. Acesso em: 03 jun. 2024.
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      Lunardi, I., Conceicao, G. J. A. da, Moran, P. J. S., & Rodrigues, J. A. R. (2005). Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum. Tetrahedron - Asymmetry, 16( 15), 2515-2519. doi:10.1016/j.tetasy.2005.06.020
    • NLM

      Lunardi I, Conceicao GJA da, Moran PJS, Rodrigues JAR. Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum [Internet]. Tetrahedron - Asymmetry. 2005 ; 16( 15): 2515-2519.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2005.06.020
    • Vancouver

      Lunardi I, Conceicao GJA da, Moran PJS, Rodrigues JAR. Highly stereoselective preparation of (3R,4S)-3,4-chromanediol by deracemization of (+-)-3-hydroxy-4-chromanone by Trichosporon cutaneum [Internet]. Tetrahedron - Asymmetry. 2005 ; 16( 15): 2515-2519.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2005.06.020
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: QUÍMICA FINA, CANDIDA, LIPASE

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      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: 03 jun. 2024.
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      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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2004.08.022
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      COSTA, Carlos E. et al. Enzymatic resolution of (RS)-p-hydroxy selenides in organic media. Tetrahedron - Asymmetry, v. 15, n. 24, p. 3945-3954, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2004.11.007. Acesso em: 03 jun. 2024.
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      Costa, C. E., Clososki, G. C., Barchesi, H. B., Zanotto, S. P., Nascimento, M. da G., & Comasseto, J. V. (2004). Enzymatic resolution of (RS)-p-hydroxy selenides in organic media. Tetrahedron - Asymmetry, 15( 24), 3945-3954. doi:10.1016/j.tetasy.2004.11.007
    • NLM

      Costa CE, Clososki GC, Barchesi HB, Zanotto SP, Nascimento M da G, Comasseto JV. Enzymatic resolution of (RS)-p-hydroxy selenides in organic media [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 24): 3945-3954.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2004.11.007
    • Vancouver

      Costa CE, Clososki GC, Barchesi HB, Zanotto SP, Nascimento M da G, Comasseto JV. Enzymatic resolution of (RS)-p-hydroxy selenides in organic media [Internet]. Tetrahedron - Asymmetry. 2004 ; 15( 24): 3945-3954.[citado 2024 jun. 03 ] Available from: https://doi.org/10.1016/j.tetasy.2004.11.007
  • 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: 03 jun. 2024.
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      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 jun. 03 ] 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 jun. 03 ] Available from: https://doi.org/10.1016/s0957-4166(03)00096-x

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