Filtros : "Indexado no Chemical Abstracts" "COMASSETO, JOAO VALDIR" Removidos: "Indexado no Pascal" "FM-MPT" "Reino Unido" "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: 11 out. 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 out. 11 ] 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 out. 11 ] 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: 11 out. 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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.09.025
  • 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: 11 out. 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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1111/j.1365-2672.2008.04097.x
  • 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: 11 out. 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
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      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 out. 11 ] 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 out. 11 ] 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: 11 out. 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 out. 11 ]
    • 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 out. 11 ]
  • 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: 11 out. 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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, CATÁLISE, TELÚRIO

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      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: 11 out. 2024.
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      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 out. 11 ]
    • 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 out. 11 ]
  • 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: 11 out. 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 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: Enzyme and Microbial Technology. Unidades: IQ, ICB, IQSC

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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      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: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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      CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol. Journal of Organometallic Chemistry, v. 691, n. 23, p. 4807-4815, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2006.05.055. Acesso em: 11 out. 2024.
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      Cunha, R. L. O. R., Zukerman-Schpector, J., Caracelli, I., & Comasseto, J. V. (2006). Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol. Journal of Organometallic Chemistry, 691( 23), 4807-4815. doi:10.1016/j.jorganchem.2006.05.055
    • NLM

      Cunha RLOR, Zukerman-Schpector J, Caracelli I, Comasseto JV. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol [Internet]. Journal of Organometallic Chemistry. 2006 ; 691( 23): 4807-4815.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.jorganchem.2006.05.055
    • Vancouver

      Cunha RLOR, Zukerman-Schpector J, Caracelli I, Comasseto JV. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol [Internet]. Journal of Organometallic Chemistry. 2006 ; 691( 23): 4807-4815.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.jorganchem.2006.05.055
  • Source: Enzyme and Microbial Technology. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, ASPERGILLUS, BIOTRANSFORMAÇÃO

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      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: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step. Journal of Organometallic Chemistry, v. 689, n. 22, p. 3631-3636, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2004.08.041. Acesso em: 11 out. 2024.
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      Cunha, R. L. O. R., Omori, Á. T., Castelani, P., Toledo, F. T., & Comasseto, J. V. (2004). One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step. Journal of Organometallic Chemistry, 689( 22), 3631-3636. doi:10.1016/j.jorganchem.2004.08.041
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      Cunha RLOR, Omori ÁT, Castelani P, Toledo FT, Comasseto JV. One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step [Internet]. Journal of Organometallic Chemistry. 2004 ; 689( 22): 3631-3636.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.jorganchem.2004.08.041
    • Vancouver

      Cunha RLOR, Omori ÁT, Castelani P, Toledo FT, Comasseto JV. One-pot synthesis of aryl butyl tellurides from tellurium tetrachloride and activated aromatics through a solventless step [Internet]. Journal of Organometallic Chemistry. 2004 ; 689( 22): 3631-3636.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.jorganchem.2004.08.041
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      CLOSOSKI, Giuliano Cesar et al. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications, v. 34, n. 5, p. 817-828, 2004Tradução . . Acesso em: 11 out. 2024.
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      Clososki, G. C., Costa, C. E., Missio, L. J., Cass, Q. B., & Comasseto, J. V. (2004). Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications, 34( 5), 817-828.
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      Clososki GC, Costa CE, Missio LJ, Cass QB, Comasseto JV. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications. 2004 ; 34( 5): 817-828.[citado 2024 out. 11 ]
    • Vancouver

      Clososki GC, Costa CE, Missio LJ, Cass QB, Comasseto JV. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications. 2004 ; 34( 5): 817-828.[citado 2024 out. 11 ]
  • Source: Synthetic Communications. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      CLOSOSKI, Giuliano Cesar e MISSIO, Lauri João e COMASSETO, João Valdir. A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications, v. 34, n. 13, p. 2371-2377, 2004Tradução . . Acesso em: 11 out. 2024.
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      Clososki, G. C., Missio, L. J., & Comasseto, J. V. (2004). A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications, 34( 13), 2371-2377.
    • NLM

      Clososki GC, Missio LJ, Comasseto JV. A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications. 2004 ; 34( 13): 2371-2377.[citado 2024 out. 11 ]
    • Vancouver

      Clososki GC, Missio LJ, Comasseto JV. A Short enantioselective synthesis of (R)-(+)-gamma-Jasmolactone. Synthetic Communications. 2004 ; 34( 13): 2371-2377.[citado 2024 out. 11 ]
  • Source: Canadian Journal of Chemistry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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      ZUKERMAN-SCHPECTOR, Júlio et al. Supramolecular self-assembly through tellurium'3 PONTOS'halogen secondary bonds: A hexagonal grid of 'Te IND. 2''Cl IND. 2' and 'Te IND. 6''Cl IND. 6' rings in the solid state structure of 1,1,3-trichloro-2,4,5,6-tetrahydro-1H-1'lâmbda'4-benzo[b]tellurophene. Canadian Journal of Chemistry, v. 80, n. 11, p. 1530-1537, 2002Tradução . . Acesso em: 11 out. 2024.
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      Zukerman-Schpector, J., Haiduc, I., Camillo, R. L., Comasseto, J. V., Cunha, R. L. O. R., & Jorge, A. (2002). Supramolecular self-assembly through tellurium'3 PONTOS'halogen secondary bonds: A hexagonal grid of 'Te IND. 2''Cl IND. 2' and 'Te IND. 6''Cl IND. 6' rings in the solid state structure of 1,1,3-trichloro-2,4,5,6-tetrahydro-1H-1'lâmbda'4-benzo[b]tellurophene. Canadian Journal of Chemistry, 80( 11), 1530-1537.
    • NLM

      Zukerman-Schpector J, Haiduc I, Camillo RL, Comasseto JV, Cunha RLOR, Jorge A. Supramolecular self-assembly through tellurium'3 PONTOS'halogen secondary bonds: A hexagonal grid of 'Te IND. 2''Cl IND. 2' and 'Te IND. 6''Cl IND. 6' rings in the solid state structure of 1,1,3-trichloro-2,4,5,6-tetrahydro-1H-1'lâmbda'4-benzo[b]tellurophene. Canadian Journal of Chemistry. 2002 ; 80( 11): 1530-1537.[citado 2024 out. 11 ]
    • Vancouver

      Zukerman-Schpector J, Haiduc I, Camillo RL, Comasseto JV, Cunha RLOR, Jorge A. Supramolecular self-assembly through tellurium'3 PONTOS'halogen secondary bonds: A hexagonal grid of 'Te IND. 2''Cl IND. 2' and 'Te IND. 6''Cl IND. 6' rings in the solid state structure of 1,1,3-trichloro-2,4,5,6-tetrahydro-1H-1'lâmbda'4-benzo[b]tellurophene. Canadian Journal of Chemistry. 2002 ; 80( 11): 1530-1537.[citado 2024 out. 11 ]
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TELÚRIO

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      VIEIRA, Maurício Leite e ZINN, Fabiano K. e COMASSETO, João Valdir. Hydrotelluration of alkynes: a unique route to Z-vinyl organometallics. Journal of the Brazilian Chemical Society, v. 12, n. 5, p. 586-596, 2001Tradução . . Disponível em: https://doi.org/10.1590/s0103-50532001000500003. Acesso em: 11 out. 2024.
    • APA

      Vieira, M. L., Zinn, F. K., & Comasseto, J. V. (2001). Hydrotelluration of alkynes: a unique route to Z-vinyl organometallics. Journal of the Brazilian Chemical Society, 12( 5), 586-596. doi:10.1590/s0103-50532001000500003
    • NLM

      Vieira ML, Zinn FK, Comasseto JV. Hydrotelluration of alkynes: a unique route to Z-vinyl organometallics [Internet]. Journal of the Brazilian Chemical Society. 2001 ; 12( 5): 586-596.[citado 2024 out. 11 ] Available from: https://doi.org/10.1590/s0103-50532001000500003
    • Vancouver

      Vieira ML, Zinn FK, Comasseto JV. Hydrotelluration of alkynes: a unique route to Z-vinyl organometallics [Internet]. Journal of the Brazilian Chemical Society. 2001 ; 12( 5): 586-596.[citado 2024 out. 11 ] Available from: https://doi.org/10.1590/s0103-50532001000500003
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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    • ABNT

      COMASSETO, João Valdir e PILLI, Ronaldo A. e SIMONELLI, Fabio. The Brazilian Meetings on Organic Synthesis (BMOS)" - uma retrospectiva. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Química, Universidade de São Paulo. Disponível em: http://www.scielo.br/pdf/jbchs/v12n5/a01v12n5.pdf. Acesso em: 11 out. 2024. , 2001
    • APA

      Comasseto, J. V., Pilli, R. A., & Simonelli, F. (2001). The Brazilian Meetings on Organic Synthesis (BMOS)" - uma retrospectiva. Journal of the Brazilian Chemical Society. São Paulo: Instituto de Química, Universidade de São Paulo. Recuperado de http://www.scielo.br/pdf/jbchs/v12n5/a01v12n5.pdf
    • NLM

      Comasseto JV, Pilli RA, Simonelli F. The Brazilian Meetings on Organic Synthesis (BMOS)" - uma retrospectiva [Internet]. Journal of the Brazilian Chemical Society. 2001 ; 12( 5):[citado 2024 out. 11 ] Available from: http://www.scielo.br/pdf/jbchs/v12n5/a01v12n5.pdf
    • Vancouver

      Comasseto JV, Pilli RA, Simonelli F. The Brazilian Meetings on Organic Synthesis (BMOS)" - uma retrospectiva [Internet]. Journal of the Brazilian Chemical Society. 2001 ; 12( 5):[citado 2024 out. 11 ] Available from: http://www.scielo.br/pdf/jbchs/v12n5/a01v12n5.pdf
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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    • ABNT

      BARRIENTOS-ASTIGARRAGA, Rafael E. et al. Carbon-carbon bond formation by means of organotellurium compounds. Journal of Organometallic Chemistry, v. 623, n. 1-2, p. 43-47, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0022-328x(00)00828-7. Acesso em: 11 out. 2024.
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      Barrientos-Astigarraga, R. E., Castelani, P., Comasseto, J. V., Formiga, H. B., Silva, N. C. da, Sumida, C. Y., & Vieira, M. L. (2001). Carbon-carbon bond formation by means of organotellurium compounds. Journal of Organometallic Chemistry, 623( 1-2), 43-47. doi:10.1016/s0022-328x(00)00828-7
    • NLM

      Barrientos-Astigarraga RE, Castelani P, Comasseto JV, Formiga HB, Silva NC da, Sumida CY, Vieira ML. Carbon-carbon bond formation by means of organotellurium compounds [Internet]. Journal of Organometallic Chemistry. 2001 ; 623( 1-2): 43-47.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/s0022-328x(00)00828-7
    • Vancouver

      Barrientos-Astigarraga RE, Castelani P, Comasseto JV, Formiga HB, Silva NC da, Sumida CY, Vieira ML. Carbon-carbon bond formation by means of organotellurium compounds [Internet]. Journal of Organometallic Chemistry. 2001 ; 623( 1-2): 43-47.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/s0022-328x(00)00828-7
  • Source: Tetrahedron: Asymmetry. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      MISSIO, Lauri João e COMASSETO, João Valdir. Enantioselective synthesis of (-)-`gamma´-jasmolactone. Tetrahedron: Asymmetry, v. 11, n. 22, p. 4609-4615, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=09574166&issue=v11i0022&article=4609_eso&form=pdf&file=file.pdf. Acesso em: 11 out. 2024.
    • APA

      Missio, L. J., & Comasseto, J. V. (2000). Enantioselective synthesis of (-)-`gamma´-jasmolactone. Tetrahedron: Asymmetry, 11( 22), 4609-4615. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=09574166&issue=v11i0022&article=4609_eso&form=pdf&file=file.pdf
    • NLM

      Missio LJ, Comasseto JV. Enantioselective synthesis of (-)-`gamma´-jasmolactone [Internet]. Tetrahedron: Asymmetry. 2000 ; 11( 22): 4609-4615.[citado 2024 out. 11 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=09574166&issue=v11i0022&article=4609_eso&form=pdf&file=file.pdf
    • Vancouver

      Missio LJ, Comasseto JV. Enantioselective synthesis of (-)-`gamma´-jasmolactone [Internet]. Tetrahedron: Asymmetry. 2000 ; 11( 22): 4609-4615.[citado 2024 out. 11 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=09574166&issue=v11i0022&article=4609_eso&form=pdf&file=file.pdf
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, FOSFATOS

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    • ABNT

      MORAES, D. N. et al. Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron, v. 56, n. 21, p. 3327-3337, 2000Tradução . . Acesso em: 11 out. 2024.
    • APA

      Moraes, D. N., Barrientos-Astigarraga, R. E., Castelani, P., & Comasseto, J. V. (2000). Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron, 56( 21), 3327-3337.
    • NLM

      Moraes DN, Barrientos-Astigarraga RE, Castelani P, Comasseto JV. Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron. 2000 ; 56( 21): 3327-3337.[citado 2024 out. 11 ]
    • Vancouver

      Moraes DN, Barrientos-Astigarraga RE, Castelani P, Comasseto JV. Addition of Z-Vinylic higher order cyanocuprates to enones followed by O-functionalization. Tetrahedron. 2000 ; 56( 21): 3327-3337.[citado 2024 out. 11 ]

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