Filtros : "Indexado no Chemical Abstracts" "COMASSETO, JOAO VALDIR" Removidos: "FM-MPT" "Financiado pela FAPDF" Limpar

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  • Source: Biotechnology Advances. Unidades: IQ, IQSC

    Subjects: QUÍMICA, ENZIMAS

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      BIROLLI, Willian Garcia et al. Biocatalysis and biotransformation in Brazil: an overview. Biotechnology Advances, v. 33, p. 481-510, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.biotechadv.2015.02.001. Acesso em: 20 jun. 2024.
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      Birolli, W. G., Ferreira , I. M., Alvarenga, N., Matos, I. L. de, Comasseto, J. V., & Porto, A. L. M. (2015). Biocatalysis and biotransformation in Brazil: an overview. Biotechnology Advances, 33, 481-510. doi:10.1016/j.biotechadv.2015.02.001
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      Birolli WG, Ferreira IM, Alvarenga N, Matos IL de, Comasseto JV, Porto ALM. Biocatalysis and biotransformation in Brazil: an overview [Internet]. Biotechnology Advances. 2015 ; 33 481-510.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.biotechadv.2015.02.001
    • Vancouver

      Birolli WG, Ferreira IM, Alvarenga N, Matos IL de, Comasseto JV, Porto ALM. Biocatalysis and biotransformation in Brazil: an overview [Internet]. Biotechnology Advances. 2015 ; 33 481-510.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.biotechadv.2015.02.001
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, SÍNTESE ORGÂNICA

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      VARGAS, Fabrício e COMASSETO, João Valdir. Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines. Journal of Organometallic Chemistry, v. 694, n. 1, p. 122-126, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.09.025. Acesso em: 20 jun. 2024.
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      Vargas, F., & Comasseto, J. V. (2009). Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines. Journal of Organometallic Chemistry, 694( 1), 122-126. doi:10.1016/j.jorganchem.2008.09.025
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      Vargas F, Comasseto JV. Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines [Internet]. Journal of Organometallic Chemistry. 2009 ; 694( 1): 122-126.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.09.025
    • Vancouver

      Vargas F, Comasseto JV. Practical synthesis of chiral 'beta'-telluro amines by ring-opening reaction of aziridines [Internet]. Journal of Organometallic Chemistry. 2009 ; 694( 1): 122-126.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.09.025
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

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      SILVA, Márcio S. e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, v. 50, n. 47, p. 6498-6501, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.09.023. Acesso em: 20 jun. 2024.
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      Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, 50( 47), 6498-6501. doi:10.1016/j.tetlet.2009.09.023
    • NLM

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
    • Vancouver

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2009.09.023
  • Source: Journal of Applied Microbiology. Unidades: IQ, IO, ICB

    Subjects: BIODEGRADAÇÃO AMBIENTAL, ESTUÁRIOS, HIDROCARBONOS

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      RODRIGUES, Débora Frigi et al. Diversity of hydrocarbon-degrading Klebsiella strains isolated from hydrocarbon-contaminated estuaries. Journal of Applied Microbiology, v. 106, n. 4, p. 1304-1314, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2672.2008.04097.x. Acesso em: 20 jun. 2024.
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      Rodrigues, D. F., Sakata, S. K., Comasseto, J. V., Bícego, M. C., & Pellizari, V. H. (2009). Diversity of hydrocarbon-degrading Klebsiella strains isolated from hydrocarbon-contaminated estuaries. Journal of Applied Microbiology, 106( 4), 1304-1314. doi:10.1111/j.1365-2672.2008.04097.x
    • NLM

      Rodrigues DF, Sakata SK, Comasseto JV, Bícego MC, Pellizari VH. Diversity of hydrocarbon-degrading Klebsiella strains isolated from hydrocarbon-contaminated estuaries [Internet]. Journal of Applied Microbiology. 2009 ; 106( 4): 1304-1314.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1111/j.1365-2672.2008.04097.x
    • Vancouver

      Rodrigues DF, Sakata SK, Comasseto JV, Bícego MC, Pellizari VH. Diversity of hydrocarbon-degrading Klebsiella strains isolated from hydrocarbon-contaminated estuaries [Internet]. Journal of Applied Microbiology. 2009 ; 106( 4): 1304-1314.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1111/j.1365-2672.2008.04097.x
  • Source: Tetrahedron Letters. Unidade: IQ

    Assunto: SÍNTESE ORGÂNICA

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      SILVA, Márcio S e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2. Tetrahedron Letters, v. 50, n. 47, p. 6498-6501, 2009Tradução . . Disponível em: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.pdf. Acesso em: 20 jun. 2024.
    • APA

      Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2. Tetrahedron Letters, 50( 47), 6498-6501. Recuperado de http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.pdf
    • NLM

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2 [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 jun. 20 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.pdf
    • Vancouver

      Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2 [Internet]. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501.[citado 2024 jun. 20 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4X66S22-3-1W&_cdi=5290&_user=5674931&_pii=S004040390901733X&_orig=browse&_coverDate=11%2F25%2F2009&_sk=999499952&view=c&wchp=dGLbVlb-zSkzV&md5=ce757759c979f22fc8e2bca9b6dd0800&ie=/sdarticle.pdf
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA

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      KEPPLER, Artur Franz et al. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, v. 50, n. 19, p. 2181-2184, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.158. Acesso em: 20 jun. 2024.
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      Keppler, A. F., Gariani, R. A., Lopes, D. G., & Comasseto, J. V. (2009). Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds. Tetrahedron Letters, 50( 19), 2181-2184. doi:10.1016/j.tetlet.2009.02.158
    • NLM

      Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
    • Vancouver

      Keppler AF, Gariani RA, Lopes DG, Comasseto JV. Lithium butylchalcogenolate induced Michael-aldol tandem sequence: easy and rapid access to highly functionalized organochalcogenides and unsaturated compounds [Internet]. Tetrahedron Letters. 2009 ; 50( 19): 2181-2184.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: COMPOSTOS ORGANOMETÁLICOS, QUÍMICA ORGÂNICA

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      PRINCIVAL, Jefferson Luiz e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, v. 46, p. 6368-6371, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.08.097. Acesso em: 20 jun. 2024.
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      Princival, J. L., Santos, A. A. dos, & Comasseto, J. V. (2009). Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones. Tetrahedron Letters, 46, 6368-6371. doi:10.1016/j.tetlet.2009.08.097
    • NLM

      Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
    • Vancouver

      Princival JL, Santos AA dos, Comasseto JV. Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones [Internet]. Tetrahedron Letters. 2009 ; 46 6368-6371.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2009.08.097
  • Source: Tetrahedron. Unidade: IQ

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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      COMASSETO, João Valdir e GARIANI, Rogério Aparecido. Biotransformations on organic selenides and tellurides: synthetic applications. Tetrahedron, v. 65, n. 41, p. 8447-8459, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2009.06.121. Acesso em: 20 jun. 2024.
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      Comasseto, J. V., & Gariani, R. A. (2009). Biotransformations on organic selenides and tellurides: synthetic applications. Tetrahedron, 65( 41), 8447-8459. doi:10.1016/j.tet.2009.06.121
    • NLM

      Comasseto JV, Gariani RA. Biotransformations on organic selenides and tellurides: synthetic applications [Internet]. Tetrahedron. 2009 ; 65( 41): 8447-8459.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tet.2009.06.121
    • Vancouver

      Comasseto JV, Gariani RA. Biotransformations on organic selenides and tellurides: synthetic applications [Internet]. Tetrahedron. 2009 ; 65( 41): 8447-8459.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tet.2009.06.121
  • Source: Tetrahedron: Asymmetry. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, LÍTIO, COMPOSTOS ORGÂNICOS

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      PRINCIVAL, Jefferson Luiz et al. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides. Tetrahedron: Asymmetry, v. 20, n. 23, p. 2699-2703, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.10.009. Acesso em: 20 jun. 2024.
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      Princival, J. L., Oliveira, M. S. C. de, Santos, A. A. dos, & Comasseto, J. V. (2009). A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides. Tetrahedron: Asymmetry, 20( 23), 2699-2703. doi:10.1016/j.tetasy.2009.10.009
    • NLM

      Princival JL, Oliveira MSC de, Santos AA dos, Comasseto JV. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 23): 2699-2703.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2009.10.009
    • Vancouver

      Princival JL, Oliveira MSC de, Santos AA dos, Comasseto JV. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 23): 2699-2703.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2009.10.009
  • Source: Tetrahedron: Asymmetry. Unidade: IQ

    Subjects: TELÚRIO, SÍNTESE ORGÂNICA

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      FERRARINI, Renan dos Santos e COMASSETO, João Valdir e SANTOS, Alcindo Aparecido dos. Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi. Tetrahedron: Asymmetry, v. 20, n. 17, p. 2043-2047, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.08.003. Acesso em: 20 jun. 2024.
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      Ferrarini, R. dos S., Comasseto, J. V., & Santos, A. A. dos. (2009). Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi. Tetrahedron: Asymmetry, 20( 17), 2043-2047. doi:10.1016/j.tetasy.2009.08.003
    • NLM

      Ferrarini R dos S, Comasseto JV, Santos AA dos. Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 17): 2043-2047.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2009.08.003
    • Vancouver

      Ferrarini R dos S, Comasseto JV, Santos AA dos. Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 17): 2043-2047.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2009.08.003
  • Source: Food and Chemical Toxicology. Unidade: IQ

    Subjects: APOPTOSE, CARCINOMA

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      ABONDANZA, T. S. et al. Bcl-2 expression and apoptosis induction in human HL60 leukaemic cells treated with a novel organotellurium(IV) compound RT-04. Food and Chemical Toxicology, v. 46, n. 7, p. 2540-2545, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2008.04.010. Acesso em: 20 jun. 2024.
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      Abondanza, T. S., Oliveira, C. R., Barbosa, C. M. V., Pereira, F. E. G., Cunha, R. L. O. R., Caires, A. C. F., et al. (2008). Bcl-2 expression and apoptosis induction in human HL60 leukaemic cells treated with a novel organotellurium(IV) compound RT-04. Food and Chemical Toxicology, 46( 7), 2540-2545. doi:10.1016/j.fct.2008.04.010
    • NLM

      Abondanza TS, Oliveira CR, Barbosa CMV, Pereira FEG, Cunha RLOR, Caires ACF, Comasseto JV, Queiroz MLS, Valadares MC, Bincoletto C. Bcl-2 expression and apoptosis induction in human HL60 leukaemic cells treated with a novel organotellurium(IV) compound RT-04 [Internet]. Food and Chemical Toxicology. 2008 ; 46( 7): 2540-2545.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.fct.2008.04.010
    • Vancouver

      Abondanza TS, Oliveira CR, Barbosa CMV, Pereira FEG, Cunha RLOR, Caires ACF, Comasseto JV, Queiroz MLS, Valadares MC, Bincoletto C. Bcl-2 expression and apoptosis induction in human HL60 leukaemic cells treated with a novel organotellurium(IV) compound RT-04 [Internet]. Food and Chemical Toxicology. 2008 ; 46( 7): 2540-2545.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.fct.2008.04.010
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, RESSONÂNCIA PARAMAGNÉTICA DE SPIN

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      KEPPLER, Artur Franz et al. Mechanistic study of the addition reaction of 'TE''CL IND. 4' to alkynes: participation of 'TE''CL IND. 3' centered-radical. Journal of Organometallic Chemistry, v. 693, n. 24, p. 3558-3562, 2008Tradução . . Acesso em: 20 jun. 2024.
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      Keppler, A. F., Prado, F. M., Cerchiaro, G., Di Mascio, P., & Comasseto, J. V. (2008). Mechanistic study of the addition reaction of 'TE''CL IND. 4' to alkynes: participation of 'TE''CL IND. 3' centered-radical. Journal of Organometallic Chemistry, 693( 24), 3558-3562.
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      Keppler AF, Prado FM, Cerchiaro G, Di Mascio P, Comasseto JV. Mechanistic study of the addition reaction of 'TE''CL IND. 4' to alkynes: participation of 'TE''CL IND. 3' centered-radical. Journal of Organometallic Chemistry. 2008 ; 693( 24): 3558-3562.[citado 2024 jun. 20 ]
    • Vancouver

      Keppler AF, Prado FM, Cerchiaro G, Di Mascio P, Comasseto JV. Mechanistic study of the addition reaction of 'TE''CL IND. 4' to alkynes: participation of 'TE''CL IND. 3' centered-radical. Journal of Organometallic Chemistry. 2008 ; 693( 24): 3558-3562.[citado 2024 jun. 20 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, TELÚRIO

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      OLIVEIRA, Roberta A. et al. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, v. 49, n. 40, p. 5759-5761, 2008Tradução . . Acesso em: 20 jun. 2024.
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      Oliveira, R. A., Oliveira, J. M., Rahmeier, L. H. S., Comasseto, J. V., Marino, J. P., & Menezes, P. H. (2008). Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters, 49( 40), 5759-5761.
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      Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 jun. 20 ]
    • Vancouver

      Oliveira RA, Oliveira JM, Rahmeier LHS, Comasseto JV, Marino JP, Menezes PH. Synthesis of the C7-C24 fragment of (-)-Macrolactin F. Tetrahedron Letters. 2008 ; 49( 40): 5759-5761.[citado 2024 jun. 20 ]
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      COMASSETO, João Valdir et al. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides. Journal of Organometallic Chemistry, v. 693, n. 17, p. 2929-2936, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.06.014. Acesso em: 20 jun. 2024.
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      Comasseto, J. V., Gariani, R. A., Princival, J. L., Dos Santos, A. A., & Zinn, F. K. (2008). Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides. Journal of Organometallic Chemistry, 693( 17), 2929-2936. doi:10.1016/j.jorganchem.2008.06.014
    • NLM

      Comasseto JV, Gariani RA, Princival JL, Dos Santos AA, Zinn FK. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides [Internet]. Journal of Organometallic Chemistry. 2008 ; 693( 17): 2929-2936.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
    • Vancouver

      Comasseto JV, Gariani RA, Princival JL, Dos Santos AA, Zinn FK. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides [Internet]. Journal of Organometallic Chemistry. 2008 ; 693( 17): 2929-2936.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS

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      TOLEDO, Fabiano Travanca et al. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, v. 49, n. 5, p. 873-875, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.11.169. Acesso em: 20 jun. 2024.
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      Toledo, F. T., Cunha, R. L. O. R., Raminelli, C., & Comasseto, J. V. (2008). Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives. Tetrahedron Letters, 49( 5), 873-875. doi:10.1016/j.tetlet.2007.11.169
    • NLM

      Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
    • Vancouver

      Toledo FT, Cunha RLOR, Raminelli C, Comasseto JV. Arylbutyltellurides as precursors of dilithium arylthienylcyanocuprates in a straightforward approach to phenethylamine derivatives [Internet]. Tetrahedron Letters. 2008 ;49( 5): 873-875.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, CATÁLISE, TELÚRIO

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    • ABNT

      GARIANI, Rogério Aparecido e DOS SANTOS, Alcindo Aparecido e COMASSETO, João Valdir. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications, v. 38, n. 5, p. 789-795, 2008Tradução . . Acesso em: 20 jun. 2024.
    • APA

      Gariani, R. A., Dos Santos, A. A., & Comasseto, J. V. (2008). In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications, 38( 5), 789-795.
    • NLM

      Gariani RA, Dos Santos AA, Comasseto JV. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications. 2008 ; 38( 5): 789-795.[citado 2024 jun. 20 ]
    • Vancouver

      Gariani RA, Dos Santos AA, Comasseto JV. In-situ generation of n-butanethiol and its reaction with electron-deficient olefins. Synthetic Communications. 2008 ; 38( 5): 789-795.[citado 2024 jun. 20 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: TELÚRIO, SÍNTESE ORGÂNICA

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      BASSORA, Bruno Karaski et al. Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, v. 48, n. 8, p. 1485-1487, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.12.063. Acesso em: 20 jun. 2024.
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      Bassora, B. K., Da Costa, C. E., Gariani, R. A., Comasseto, J. V., & Dos Santos, A. A. (2007). Tellurium in organic synthesis: synthesis of bioactive butenolides. Tetrahedron Letters, 48( 8), 1485-1487. doi:10.1016/j.tetlet.2006.12.063
    • NLM

      Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
    • Vancouver

      Bassora BK, Da Costa CE, Gariani RA, Comasseto JV, Dos Santos AA. Tellurium in organic synthesis: synthesis of bioactive butenolides [Internet]. Tetrahedron Letters. 2007 ; 48( 8): 1485-1487.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2006.12.063
  • Source: Enzyme and Microbial Technology. Unidades: ICB, IQ, IQSC

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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      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: 20 jun. 2024.
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      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. 20 ] 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. 20 ] 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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      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: 20 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. 20 ] 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. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: Tetrahedron. Unidade: IQ

    Subjects: CATÁLISE, REAGENTES ORGÂNICOS

    Acesso à fonteDOIHow to cite
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    • ABNT

      RAMINELLI, Cristiano et al. The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes. Tetrahedron, v. 63, n. 36, p. 8801-8809, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.06.057. Acesso em: 20 jun. 2024.
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      Raminelli, C., Gargalaka Júnior, J., Silveira, C. da C., & Comasseto, J. V. (2007). The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes. Tetrahedron, 63( 36), 8801-8809. doi:10.1016/j.tet.2007.06.057
    • NLM

      Raminelli C, Gargalaka Júnior J, Silveira C da C, Comasseto JV. The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes [Internet]. Tetrahedron. 2007 ; 63( 36): 8801-8809.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tet.2007.06.057
    • Vancouver

      Raminelli C, Gargalaka Júnior J, Silveira C da C, Comasseto JV. The coupling of butylvinyltellurides with organometallic reagents catalysed by nickel complexes [Internet]. Tetrahedron. 2007 ; 63( 36): 8801-8809.[citado 2024 jun. 20 ] Available from: https://doi.org/10.1016/j.tet.2007.06.057

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