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

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  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: LÍTIO, CALCOGÊNIOS, SÍNTESE ORGÂNICA

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    • ABNT

      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: REAGENTES ORGÂNICOS, TELÚRIO

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    • ABNT

      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: 11 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. 11 ]
    • 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. 11 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS

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    • ABNT

      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: 11 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. 11 ] 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. 11 ] 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: 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
    • 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. 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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    • ABNT

      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.
    • APA

      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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    • 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: 11 out. 2024.
    • APA

      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. 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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    • ABNT

      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
    • 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. 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: 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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    • ABNT

      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.
    • APA

      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. 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: 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.
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      Dos Santos, A. A., Da Costa, C. E., Princival, J. L., & Comasseto, J. V. (2006). Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides. Tetrahedron - Asymmetry, 17( 15), 2252-2259. doi:10.1016/j.tetasy.2006.07.024
    • NLM

      Dos Santos AA, Da Costa CE, Princival JL, Comasseto JV. Lipase-catalyzed kinetic resolution of (RS)-hydroxy tellurides [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 15): 2252-2259.[citado 2024 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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      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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      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.
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      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 ]
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, REAGENTES ORGÂNICOS

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      DOS SANTOS, Alcindo Aparecido et al. Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron, v. 61, n. 38, p. 9173-9179, 2005Tradução . . Acesso em: 11 out. 2024.
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      Dos Santos, A. A., Castelani, P., Bassora, B. K., Fogo Junior, J. C., Costa, C. E. da, & Comasseto, J. V. (2005). Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron, 61( 38), 9173-9179.
    • NLM

      Dos Santos AA, Castelani P, Bassora BK, Fogo Junior JC, Costa CE da, Comasseto JV. Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron. 2005 ; 61( 38): 9173-9179.[citado 2024 out. 11 ]
    • Vancouver

      Dos Santos AA, Castelani P, Bassora BK, Fogo Junior JC, Costa CE da, Comasseto JV. Chemoselective reduction of beta-butyltellanyl 'alpha','beta'-unsaturated carbonyl compounds to allylic alcohols. Tetrahedron. 2005 ; 61( 38): 9173-9179.[citado 2024 out. 11 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA

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      CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. Selectivity aspects of the ring opening reaction of 2-alkenyl aziridines by carbon nucleophiles. Tetrahedron Letters, v. 46, n. 15, p. 2539-2542, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2005.02.089. Acesso em: 11 out. 2024.
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      Cunha, R. L. O. R., Diego, D. G., Simonelli, F., & Comasseto, J. V. (2005). Selectivity aspects of the ring opening reaction of 2-alkenyl aziridines by carbon nucleophiles. Tetrahedron Letters, 46( 15), 2539-2542. doi:10.1016/j.tetlet.2005.02.089
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      Cunha RLOR, Diego DG, Simonelli F, Comasseto JV. Selectivity aspects of the ring opening reaction of 2-alkenyl aziridines by carbon nucleophiles [Internet]. Tetrahedron Letters. 2005 ; 46( 15): 2539-2542.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2005.02.089
    • Vancouver

      Cunha RLOR, Diego DG, Simonelli F, Comasseto JV. Selectivity aspects of the ring opening reaction of 2-alkenyl aziridines by carbon nucleophiles [Internet]. Tetrahedron Letters. 2005 ; 46( 15): 2539-2542.[citado 2024 out. 11 ] Available from: https://doi.org/10.1016/j.tetlet.2005.02.089
  • 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

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