Filtros : "Indexado no Chemical Abstracts" "COMASSETO, JOAO VALDIR" Removidos: "FM-MPT" "Reino Unido" "2008" "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: 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: 11 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. 11 ] 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. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.158
  • 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: 11 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
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      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. 11 ] 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. 11 ] 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: 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: 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: 11 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. 11 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
    • Vancouver

      Omori ÁT, Assis LF, Andrade LH, Comasseto JV, Porto ALM. Enantiomerically pure organoseleno-1-arylethanols by enzymatic resolution with Candida antarctica lipase: Novozym 435 [Internet]. Tetrahedron - Asymmetry. 2007 ; 18( 9): 1048-1053.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tetasy.2007.04.019
  • Source: 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: 11 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
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      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. 11 ] 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. 11 ] 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: 11 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
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      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. 11 ] 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. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
  • 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: 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: 11 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. 11 ] 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. 11 ] 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: 11 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
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      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. 11 ] 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. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2007.05.074
  • 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
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      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: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TELÚRIO, LÍTIO

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      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: 11 out. 2024.
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      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. 11 ] 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. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: FEROMÔNIOS, SÍNTESE ORGÂNICA, TELÚRIO

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      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: 11 out. 2024.
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      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. 11 ] 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. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2006.08.005
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: LIPASE, QUÍMICA ORGÂNICA

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      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: 11 out. 2024.
    • APA

      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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
  • Source: Tetrahedron - Asymmetry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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    • ABNT

      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: 11 out. 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 out. 11 ] 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 out. 11 ] Available from: https://doi.org/10.1016/j.tetasy.2006.10.034
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TELÚRIO, LÍTIO

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    • ABNT

      PRINCIVAL, Jefferson Luiz et al. 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters, v. 46, n. 26, p. 4423-4425, 2005Tradução . . Acesso em: 11 out. 2024.
    • APA

      Princival, J. L., Barros, S. M. G. de, Comasseto, J. V., & Dos Santos, A. A. (2005). 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters, 46( 26), 4423-4425.
    • NLM

      Princival JL, Barros SMG de, Comasseto JV, Dos Santos AA. 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters. 2005 ; 46( 26): 4423-4425.[citado 2024 out. 11 ]
    • Vancouver

      Princival JL, Barros SMG de, Comasseto JV, Dos Santos AA. 'gamma'-butyltelluro-2-butanol: a route to reactive 1,4-dianion intermediates. Tetrahedron Letters. 2005 ; 46( 26): 4423-4425.[citado 2024 out. 11 ]
  • Source: Tetrahedron. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA

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

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

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

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, TELÚRIO, REAGENTES ORGÂNICOS

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    • ABNT

      CASTELANI, Priscila e COMASSETO, João Valdir. Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron, v. 61, n. 9, p. 2319-2326, 2005Tradução . . Acesso em: 11 out. 2024.
    • APA

      Castelani, P., & Comasseto, J. V. (2005). Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron, 61( 9), 2319-2326.
    • NLM

      Castelani P, Comasseto JV. Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron. 2005 ; 61( 9): 2319-2326.[citado 2024 out. 11 ]
    • Vancouver

      Castelani P, Comasseto JV. Diastereoselective synthesis of 'alpha','beta'-unsaturated systems. Tetrahedron. 2005 ; 61( 9): 2319-2326.[citado 2024 out. 11 ]

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