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  • 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: 31 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
    • NLM

      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. 31 ] 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. 31 ] 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: 31 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. 31 ] 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. 31 ] Available from: https://doi.org/10.1111/j.1365-2672.2008.04097.x
  • 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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
  • 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: 31 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
    • 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 out. 31 ] 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. 31 ] 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: 31 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.
    • NLM

      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. 31 ]
    • 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. 31 ]
  • 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: 31 out. 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.
    • NLM

      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 out. 31 ]
    • 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 out. 31 ]
  • 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: 31 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. 31 ] 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. 31 ] 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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2007.11.169
  • 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: 31 out. 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 out. 31 ] 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 out. 31 ] 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: 31 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. 31 ] 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. 31 ] 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: 31 out. 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 out. 31 ] 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. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: Tetrahedron. Unidade: IQ

    Subjects: CATÁLISE, REAGENTES ORGÂNICOS

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      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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1016/j.tet.2007.06.057
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      TOLEDO, Fabiano Travanca et al. The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, v. 48, n. 46, p. 8125-8127, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.09.111. Acesso em: 31 out. 2024.
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      Toledo, F. T., Marques, H., Comasseto, J. V., & Raminelli, C. (2007). The diorgano dichalcogenides addition to benzyne under mild conditions. Tetrahedron Letters, 48( 46), 8125-8127. doi:10.1016/j.tetlet.2007.09.111
    • NLM

      Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
    • Vancouver

      Toledo FT, Marques H, Comasseto JV, Raminelli C. The diorgano dichalcogenides addition to benzyne under mild conditions [Internet]. Tetrahedron Letters. 2007 ; 48( 46): 8125-8127.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
  • Source: Journal of Molecular Catalysis B - Enzymatic. Unidades: IQ, IQSC

    Subjects: BIOTRANSFORMAÇÃO, ASPERGILLUS

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      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: 31 out. 2024.
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      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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1016/j.molcatb.2007.01.004
  • Source: Tetrahedron. Unidade: IQ

    Subjects: TELÚRIO, LÍTIO, SÍNTESE ORGÂNICA

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      DOS SANTOS, Alcindo Aparecido et al. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems. Tetrahedron, v. 63, n. 24, p. 5167-5172, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2007.03.178. Acesso em: 31 out. 2024.
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      Dos Santos, A. A., Princival, J. L., Comasseto, J. V., Barros, S. M. G. de, & Brainer Neto, J. E. (2007). Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems. Tetrahedron, 63( 24), 5167-5172. doi:10.1016/j.tet.2007.03.178
    • NLM

      Dos Santos AA, Princival JL, Comasseto JV, Barros SMG de, Brainer Neto JE. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems [Internet]. Tetrahedron. 2007 ; 63( 24): 5167-5172.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tet.2007.03.178
    • Vancouver

      Dos Santos AA, Princival JL, Comasseto JV, Barros SMG de, Brainer Neto JE. Tellurium/lithium exchange reactions in the synthesis of spiroketals and 1,6-dioxygenated systems [Internet]. Tetrahedron. 2007 ; 63( 24): 5167-5172.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tet.2007.03.178
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: LÍTIO, SÍNTESE ORGÂNICA

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      SILVEIRA, Claudio da Cruz e GUERRA, Robson Brum e COMASSETO, João Valdir. Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates. Tetrahedron Letters, v. 48, n. 29, p. 5121-5124, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.05.074. Acesso em: 31 out. 2024.
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      Silveira, C. da C., Guerra, R. B., & Comasseto, J. V. (2007). Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates. Tetrahedron Letters, 48( 29), 5121-5124. doi:10.1016/j.tetlet.2007.05.074
    • NLM

      Silveira C da C, Guerra RB, Comasseto JV. Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates [Internet]. Tetrahedron Letters. 2007 ; 48( 29): 5121-5124.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2007.05.074
    • Vancouver

      Silveira C da C, Guerra RB, Comasseto JV. Stereoselective synthesis of vinylic chalcogenides through vinylic substitution by lithium organylchalcogenolates [Internet]. Tetrahedron Letters. 2007 ; 48( 29): 5121-5124.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2007.05.074
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: BOTÂNICA, QUÍMICA

    Acesso à fonteAcesso à fonteDOIHow to cite
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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: 31 out. 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 out. 31 ] 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 out. 31 ] Available from: https://doi.org/10.1016/j.tetasy.2007.05.036
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      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: 31 out. 2024.
    • APA

      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. 31 ] 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. 31 ] Available from: https://doi.org/10.1016/j.jorganchem.2006.05.055
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TELÚRIO, LÍTIO

    Acesso à fonteDOIHow to cite
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    • ABNT

      DOS SANTOS, Alcindo Aparecido et al. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, v. 47, n. 50, p. 8933-8935, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.10.039. Acesso em: 31 out. 2024.
    • APA

      Dos Santos, A. A., Ferrarini, R. dos S., Princival, J. L., & Comasseto, J. V. (2006). Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, 47( 50), 8933-8935. doi:10.1016/j.tetlet.2006.10.039
    • NLM

      Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
    • Vancouver

      Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: FEROMÔNIOS, SÍNTESE ORGÂNICA, TELÚRIO

    Acesso à fonteDOIHow to cite
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    • ABNT

      DIEGO, Dennis Galasso e CUNHA, Rodrigo Luiz Oliveira Rodrigues e COMASSETO, João Valdir. Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones. Tetrahedron Letters, v. 47, n. 40, p. 7147-7148, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.08.005. Acesso em: 31 out. 2024.
    • APA

      Diego, D. G., Cunha, R. L. O. R., & Comasseto, J. V. (2006). Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones. Tetrahedron Letters, 47( 40), 7147-7148. doi:10.1016/j.tetlet.2006.08.005
    • NLM

      Diego DG, Cunha RLOR, Comasseto JV. Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones [Internet]. Tetrahedron Letters. 2006 ; 47( 40): 7147-7148.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2006.08.005
    • Vancouver

      Diego DG, Cunha RLOR, Comasseto JV. Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones [Internet]. Tetrahedron Letters. 2006 ; 47( 40): 7147-7148.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.tetlet.2006.08.005

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