Filtros : "Indexado no Research Alert" "QUÍMICA ORGÂNICA" Removido: "BIANCHI, MARCELO BELENTANI DE" Limpar

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  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: QUÍMICA ORGÂNICA, DERMATOLOGIA, TOXICOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S52-S99, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.10.042. Acesso em: 20 ago. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2012). A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, 50, S52-S99. doi:10.1016/j.fct.2011.10.042
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
  • Source: Synthesis. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TÁLIO, NITRATOS, CARBONO

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      FERRAZ, Helena Maria Carvalho e CARNEIRO, Vânia Maria Teixeira e SILVA JUNIOR, Luiz Fernando da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, n. 3, p. 385-388, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf. Acesso em: 20 ago. 2024.
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      Ferraz, H. M. C., Carneiro, V. M. T., & Silva Junior, L. F. da. (2009). Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes. Synthesis, ( 3), 385-388. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
    • NLM

      Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 ago. 20 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
    • Vancouver

      Ferraz HMC, Carneiro VMT, Silva Junior LF da. Ring contraction of 1,2-dihydronaphthalenes promoted by thallium(III) in acetonitrile: a diastereoselective approach to indanes [Internet]. Synthesis. 2009 ;( 3): 385-388.[citado 2024 ago. 20 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synthesis/doi/10.1055/s-0028-1083308.pdf
  • Source: Tetrahedron Asymmetry. Unidade: IQ

    Subjects: ASPERGILLUS, QUÍMICA ORGÂNICA

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      ANDRADE, Leandro Helgueira e PIOVAN, Leandro e PASQUINI, Mônica D`Arcadia. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, v. 20, n. 13, p. 1521-1525, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.05.033. Acesso em: 20 ago. 2024.
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      Andrade, L. H., Piovan, L., & Pasquini, M. D. `A. (2009). Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent. Tetrahedron Asymmetry, 20( 13), 1521-1525. doi:10.1016/j.tetasy.2009.05.033
    • NLM

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
    • Vancouver

      Andrade LH, Piovan L, Pasquini MD`A. Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus and Rhizopus oryzae: the role of glycerol as a co-solvent [Internet]. Tetrahedron Asymmetry. 2009 ; 20( 13): 1521-1525.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2009.05.033
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      SILVA JR., Luiz Fernando da e QUINTILIANO, Samir Augusto Pino. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, v. 50, n. 19, p. 2256-2260, 2009Tradução . . Acesso em: 20 ago. 2024.
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      Silva Jr., L. F. da, & Quintiliano, S. A. P. (2009). An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters, 50( 19), 2256-2260.
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      Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 ago. 20 ]
    • Vancouver

      Silva Jr. LF da, Quintiliano SAP. An expeditious synthesis of hexahydrobenzol [f]isoquinoline and of hexahydrobenzol[f]isoquinoline via iodine-catalyzed prins and aza-prins cyclization. Tetrahedron Letters. 2009 ; 50( 19): 2256-2260.[citado 2024 ago. 20 ]
  • Source: Bioorganic & Medicinal Chemistry Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, PEROXIDASE

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      MALVEZZI, Alberto et al. Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, v. 18, n. 1, p. 350-354, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2007.10.068. Acesso em: 20 ago. 2024.
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      Malvezzi, A., Rezende, L. de, Izidoro, M. A., Cezari, M. H. S., Juliano, L., & Amaral, A. T. do. (2008). Uncovering false positives on a virtual screening search for cruzain inhibitors. Bioorganic & Medicinal Chemistry Letters, 18( 1), 350-354. doi:10.1016/j.bmcl.2007.10.068
    • NLM

      Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
    • Vancouver

      Malvezzi A, Rezende L de, Izidoro MA, Cezari MHS, Juliano L, Amaral AT do. Uncovering false positives on a virtual screening search for cruzain inhibitors [Internet]. Bioorganic & Medicinal Chemistry Letters. 2008 ; 18( 1): 350-354.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.bmcl.2007.10.068
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      COMASSETO, João Valdir et al. Hydrochalcogenation of activated olefines. Synthesis of functionalized dialkylchalcogenides. Journal of Organometallic Chemistry, v. 693, n. 17, p. 2929-2936, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2008.06.014. Acesso em: 20 ago. 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 ago. 20 ] Available from: https://doi.org/10.1016/j.jorganchem.2008.06.014
    • Vancouver

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

    Subjects: BIOTRANSFORMAÇÃO, QUÍMICA ORGÂNICA

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      RAMINELLI, Cristiano et al. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435). Enzyme and Microbial Technology, v. 40, n. 2, p. 362-369, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2006.06.002. Acesso em: 20 ago. 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 ago. 20 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
    • Vancouver

      Raminelli C, Kagohara E, Pellizari VH, Comasseto JV, Andrade LH, Porto ALM. Biotransformations of Mannich bases and propiophenones by Brazilian microorganisms and enzymatic resolution of phenylpropanols by lipase from Candida antarctica (Novozym 435) [Internet]. Enzyme and Microbial Technology. 2007 ; 40( 2): 362-369.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.enzmictec.2006.06.002
  • Source: Food and Chemical Toxicology. Unidade: IQ

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA

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      VALADARES, Marize Campos et al. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide. Food and Chemical Toxicology, v. 45, n. 10, p. 1975-1978, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2007.04.016. Acesso em: 20 ago. 2024.
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      Valadares, M. C., Rezende, K. R., Pereira, E. R. T., Sousa, M. C. de, Gonçalves Santiago, B., Assis, J. C. de, & Kato, M. J. (2007). Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide. Food and Chemical Toxicology, 45( 10), 1975-1978. doi:10.1016/j.fct.2007.04.016
    • NLM

      Valadares MC, Rezende KR, Pereira ERT, Sousa MC de, Gonçalves Santiago B, Assis JC de, Kato MJ. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide [Internet]. Food and Chemical Toxicology. 2007 ; 45( 10): 1975-1978.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.fct.2007.04.016
    • Vancouver

      Valadares MC, Rezende KR, Pereira ERT, Sousa MC de, Gonçalves Santiago B, Assis JC de, Kato MJ. Protective effects of 4-nerolidylcatechol against genotoxicity induced by cyclophosphamide [Internet]. Food and Chemical Toxicology. 2007 ; 45( 10): 1975-1978.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.fct.2007.04.016
  • 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: 20 ago. 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 ago. 20 ] 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 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2007.09.111
  • Source: Synthesis. Unidade: IQ

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA

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      FERRAZ, Helena Maria Carvalho e BOMBONATO, Fernanda Irene e LONGO JUNIOR, Luiz Sidney. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, n. 21, p. 3261-3285, 2007Tradução . . Acesso em: 20 ago. 2024.
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      Ferraz, H. M. C., Bombonato, F. I., & Longo Junior, L. S. (2007). Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis, ( 21), 3261-3285.
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      Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 ago. 20 ]
    • Vancouver

      Ferraz HMC, Bombonato FI, Longo Junior LS. Synthetic approaches to naturally occurring ten-membered-ring lactones. Synthesis. 2007 ;( 21): 3261-3285.[citado 2024 ago. 20 ]
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: COMPOSTOS ORGÂNICOS, QUÍMICA ORGÂNICA

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      MARZORATI, Liliana et al. New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, v. 48, n. 37, p. 6509-6513, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2007.07.054. Acesso em: 20 ago. 2024.
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      Marzorati, L., Barazzone, G. C., Bueno Filho, M. A., Wladislaw, B., & Di Vitta, C. (2007). New methodology for the preparation of N-tosyl aziridine-2-carboxylates. Tetrahedron Letters, 48( 37), 6509-6513. doi:10.1016/j.tetlet.2007.07.054
    • NLM

      Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
    • Vancouver

      Marzorati L, Barazzone GC, Bueno Filho MA, Wladislaw B, Di Vitta C. New methodology for the preparation of N-tosyl aziridine-2-carboxylates [Internet]. Tetrahedron Letters. 2007 ; 48( 37): 6509-6513.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2007.07.054
  • 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: 20 ago. 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 ago. 20 ] 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 ago. 20 ] 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: 20 ago. 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
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      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 ago. 20 ] 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 ago. 20 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
  • Source: Zeitschrift für Kristallographie - New Crystal Structures. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      ZUKERMAN-SCHPECTOR, Júlio et al. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures, v. 221, n. 3, p. 311-312, 2006Tradução . . Acesso em: 20 ago. 2024.
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      Zukerman-Schpector, J., Silva, R. O. da, Olivato, P. R., Vinhato, E., Rodrigues, A., & Cerqueira Júnior, C. R. (2006). Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures, 221( 3), 311-312.
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      Zukerman-Schpector J, Silva RO da, Olivato PR, Vinhato E, Rodrigues A, Cerqueira Júnior CR. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 3): 311-312.[citado 2024 ago. 20 ]
    • Vancouver

      Zukerman-Schpector J, Silva RO da, Olivato PR, Vinhato E, Rodrigues A, Cerqueira Júnior CR. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 3): 311-312.[citado 2024 ago. 20 ]
  • 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: 20 ago. 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
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      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 ago. 20 ] 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 ago. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.024
  • Source: Synthesis. Unidade: IQ

    Subjects: TÁLIO, QUÍMICA ORGÂNICA

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      FERRAZ, Helena Maria Carvalho e VIEIRA, Tiago O. e SILVA JR., Luiz Fernando da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, n. 16, p. 2748-2752, 2006Tradução . . Acesso em: 20 ago. 2024.
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      Ferraz, H. M. C., Vieira, T. O., & Silva Jr., L. F. da. (2006). Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis, ( 16), 2748-2752.
    • NLM

      Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 ago. 20 ]
    • Vancouver

      Ferraz HMC, Vieira TO, Silva Jr. LF da. Thallium(III)-mediated ring contraction of cis-octalins: an approach for the diastereoselective construction of the nor-bakkane skeleton. Synthesis. 2006 ;( 16): 2748-2752.[citado 2024 ago. 20 ]
  • Source: Synthesis. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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    • ABNT

      BASTOS, Erick Leite et al. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane]. Synthesis, n. 15, p. , 2006Tradução . . Disponível em: https://doi.org/10.1055/s-2006-942357. Acesso em: 20 ago. 2024.
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      Bastos, E. L., Ciscato, L. F. M. L., Weiss, D., Beckert, R., & Baader, W. J. (2006). Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane]. Synthesis, ( 15), . doi:10.1055/s-2006-942357
    • NLM

      Bastos EL, Ciscato LFML, Weiss D, Beckert R, Baader WJ. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane] [Internet]. Synthesis. 2006 ;( 15): .[citado 2024 ago. 20 ] Available from: https://doi.org/10.1055/s-2006-942357
    • Vancouver

      Bastos EL, Ciscato LFML, Weiss D, Beckert R, Baader WJ. Comparison of convenient alternative synthetic approaches to 4-[(3-tert-Butyldimethylsilyloxy)phenyl]-4-methoxyspiro[1,2-dioxetane-3,2 '-adamantane] [Internet]. Synthesis. 2006 ;( 15): .[citado 2024 ago. 20 ] Available from: https://doi.org/10.1055/s-2006-942357
  • Source: Tetrahedron - Asymmetry. Unidades: IQ, IQSC

    Subjects: CANDIDA, QUÍMICA ORGÂNICA

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      VIEIRA, Tiago de Oliveira et al. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, v. 17, n. 13, p. 1990-1994, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2006.07.014. Acesso em: 20 ago. 2024.
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      Vieira, T. de O., Ferraz, H. M. C., Andrade, L. H., & Porto, A. L. M. (2006). Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435). Tetrahedron - Asymmetry, 17( 13), 1990-1994. doi:10.1016/j.tetasy.2006.07.014
    • NLM

      Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
    • Vancouver

      Vieira T de O, Ferraz HMC, Andrade LH, Porto ALM. Highly enantioselective enzymatic resolution of cis-fused octalols mediated by Candida antarctica lipase (Novozym 435) [Internet]. Tetrahedron - Asymmetry. 2006 ; 17( 13): 1990-1994.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tetasy.2006.07.014
  • Source: Tetrahedron. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      NIHEI, Ken-ichi et al. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, v. 62, n. 35, p. 8335-8350, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.06.051. Acesso em: 20 ago. 2024.
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      Nihei, K. -ichi, Kato, M. J., Yamane, T., & Konno, K. (2006). An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins. Tetrahedron, 62( 35), 8335-8350. doi:10.1016/j.tet.2006.06.051
    • NLM

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
    • Vancouver

      Nihei K-ichi, Kato MJ, Yamane T, Konno K. An efficient and versatile synthesis of all structural types of acylpolyamine spider toxins [Internet]. Tetrahedron. 2006 ; 62( 35): 8335-8350.[citado 2024 ago. 20 ] Available from: https://doi.org/10.1016/j.tet.2006.06.051
  • Source: Zeitschrift für Kristallographie - New Crystal Structures. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      ZUKERMAN-SCHPECTOR, Júlio et al. Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures, v. 221, n. 2, p. 165-166, 2006Tradução . . Acesso em: 20 ago. 2024.
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      Zukerman-Schpector, J., Maganhi, S. H., Olivato, P. R., Vinhato, E., & Cerqueira Júnior, C. R. (2006). Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures, 221( 2), 165-166.
    • NLM

      Zukerman-Schpector J, Maganhi SH, Olivato PR, Vinhato E, Cerqueira Júnior CR. Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 2): 165-166.[citado 2024 ago. 20 ]
    • Vancouver

      Zukerman-Schpector J, Maganhi SH, Olivato PR, Vinhato E, Cerqueira Júnior CR. Crystal structure of cis-4-tert-butyl-2-(4-nitrophenylsulfonyl)cyclohexanone, 'C IND. 16''H IND. 21''NO IND. 5'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 2): 165-166.[citado 2024 ago. 20 ]

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