Filtros : "Burtoloso, Antonio Carlos Bender" "Alemanha" Limpar

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  • Source: Synthesis: reviews and full papers in chemical synthesis. Unidade: IQSC

    Subjects: ACILAÇÃO, ENXOFRE

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      MIZOBUCHI, Eduardo F. e BURTOLOSO, Antonio Carlos Bender. The acylation of @-carbonyl sulfoxonium ylides with N-hydroxyphthalimide esters. Synthesis: reviews and full papers in chemical synthesis, v. 56, p. A–H, 2024Tradução . . Disponível em: https://doi.org/10.1055/a-2412-9549. Acesso em: 16 nov. 2024.
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      Mizobuchi, E. F., & Burtoloso, A. C. B. (2024). The acylation of @-carbonyl sulfoxonium ylides with N-hydroxyphthalimide esters. Synthesis: reviews and full papers in chemical synthesis, 56, A–H. doi:10.1055/a-2412-9549
    • NLM

      Mizobuchi EF, Burtoloso ACB. The acylation of @-carbonyl sulfoxonium ylides with N-hydroxyphthalimide esters [Internet]. Synthesis: reviews and full papers in chemical synthesis. 2024 ;56 A–H.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/a-2412-9549
    • Vancouver

      Mizobuchi EF, Burtoloso ACB. The acylation of @-carbonyl sulfoxonium ylides with N-hydroxyphthalimide esters [Internet]. Synthesis: reviews and full papers in chemical synthesis. 2024 ;56 A–H.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/a-2412-9549
  • Source: Chemistry: An Asian Journal. Unidade: IQSC

    Subjects: ENXOFRE, QUÍMICA ORGÂNICA

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      JESUS, Matheus Pereira de e BURTOLOSO, Antonio Carlos Bender. Revisiting the reaction of sulfur ylides with acetylenic esters: Synthesis of trisubstituted 1,3-dienes, α-carbonyl vinyl sulfoxides and α-carbonyl vinyl sulfoxonium ylides. Chemistry: An Asian Journal, p. e20240093, 2024Tradução . . Disponível em: https://doi.org//10.1002/asia.20240093. Acesso em: 16 nov. 2024.
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      Jesus, M. P. de, & Burtoloso, A. C. B. (2024). Revisiting the reaction of sulfur ylides with acetylenic esters: Synthesis of trisubstituted 1,3-dienes, α-carbonyl vinyl sulfoxides and α-carbonyl vinyl sulfoxonium ylides. Chemistry: An Asian Journal, e20240093. doi:10.1002/asia.20240093
    • NLM

      Jesus MP de, Burtoloso ACB. Revisiting the reaction of sulfur ylides with acetylenic esters: Synthesis of trisubstituted 1,3-dienes, α-carbonyl vinyl sulfoxides and α-carbonyl vinyl sulfoxonium ylides [Internet]. Chemistry: An Asian Journal. 2024 ; e20240093.[citado 2024 nov. 16 ] Available from: https://doi.org//10.1002/asia.20240093
    • Vancouver

      Jesus MP de, Burtoloso ACB. Revisiting the reaction of sulfur ylides with acetylenic esters: Synthesis of trisubstituted 1,3-dienes, α-carbonyl vinyl sulfoxides and α-carbonyl vinyl sulfoxonium ylides [Internet]. Chemistry: An Asian Journal. 2024 ; e20240093.[citado 2024 nov. 16 ] Available from: https://doi.org//10.1002/asia.20240093
  • Source: Chemistry: A European Journal. Unidade: IQSC

    Subjects: FLÚOR, QUÍMICA ORGÂNICA

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      HAYASHI, Marcio e BURTOLOSO, Antonio Carlos Bender. Synthesis of gem-Difluorinated Keto-Sulfoxides from Sulfoxonium Ylides. Chemistry: A European Journal, p. e202400108, 2024Tradução . . Disponível em: https://doi.org/10.1002/chem.202400108. Acesso em: 16 nov. 2024.
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      Hayashi, M., & Burtoloso, A. C. B. (2024). Synthesis of gem-Difluorinated Keto-Sulfoxides from Sulfoxonium Ylides. Chemistry: A European Journal, e202400108. doi:10.1002/chem.202400108
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      Hayashi M, Burtoloso ACB. Synthesis of gem-Difluorinated Keto-Sulfoxides from Sulfoxonium Ylides [Internet]. Chemistry: A European Journal. 2024 ;e202400108.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chem.202400108
    • Vancouver

      Hayashi M, Burtoloso ACB. Synthesis of gem-Difluorinated Keto-Sulfoxides from Sulfoxonium Ylides [Internet]. Chemistry: A European Journal. 2024 ;e202400108.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chem.202400108
  • Source: Advanced Synthesis & Catalysis. Unidade: IQSC

    Subjects: COBRE, IODO

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      PEREZ, Radell Echemendía e MURPHY, Graham K. e BURTOLOSO, Antonio Carlos Bender. Copper-Catalyzed α-Arylation of Sulfoxonium Ylides Using Hypervalent Iodine Compounds. Advanced Synthesis & Catalysis, v. 366, p. 396-401, 2024Tradução . . Disponível em: https://doi.org/10.1002/adsc.202301061. Acesso em: 16 nov. 2024.
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      Perez, R. E., Murphy, G. K., & Burtoloso, A. C. B. (2024). Copper-Catalyzed α-Arylation of Sulfoxonium Ylides Using Hypervalent Iodine Compounds. Advanced Synthesis & Catalysis, 366, 396-401. doi:10.1002/adsc.202301061
    • NLM

      Perez RE, Murphy GK, Burtoloso ACB. Copper-Catalyzed α-Arylation of Sulfoxonium Ylides Using Hypervalent Iodine Compounds [Internet]. Advanced Synthesis & Catalysis. 2024 ; 366 396-401.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/adsc.202301061
    • Vancouver

      Perez RE, Murphy GK, Burtoloso ACB. Copper-Catalyzed α-Arylation of Sulfoxonium Ylides Using Hypervalent Iodine Compounds [Internet]. Advanced Synthesis & Catalysis. 2024 ; 366 396-401.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/adsc.202301061
  • Source: Synthesis. Unidade: IQSC

    Subjects: ENXOFRE, ACILAÇÃO, CETONA

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      SOUZA, João H. de e VARGAS, Jorge Andres Mora e BURTOLOSO, Antonio Carlos Bender. An Improved Protocol for the Synthesis of Carbonyl Sulfoxonium Ylides. Synthesis, v. 35, p. 758–762, 2024Tradução . . Disponível em: https://doi.org/10.1055/a-2222-3695. Acesso em: 16 nov. 2024.
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      Souza, J. H. de, Vargas, J. A. M., & Burtoloso, A. C. B. (2024). An Improved Protocol for the Synthesis of Carbonyl Sulfoxonium Ylides. Synthesis, 35, 758–762. doi:10.1055/a-2222-3695
    • NLM

      Souza JH de, Vargas JAM, Burtoloso ACB. An Improved Protocol for the Synthesis of Carbonyl Sulfoxonium Ylides [Internet]. Synthesis. 2024 ;35 758–762.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/a-2222-3695
    • Vancouver

      Souza JH de, Vargas JAM, Burtoloso ACB. An Improved Protocol for the Synthesis of Carbonyl Sulfoxonium Ylides [Internet]. Synthesis. 2024 ;35 758–762.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/a-2222-3695
  • Source: ChemSusChem. Unidade: IQSC

    Subjects: GÁS CARBÔNICO, POLÍMEROS (QUÍMICA ORGÂNICA)

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      VARGAS, Jorge Andres Mora e BURTOLOSO, Antonio Carlos Bender. CO2-Based Carbamate Synthesis Utilizing Reusable Polymer-Supported DBU. ChemSusChem, p. e202300936, 2023Tradução . . Disponível em: https://doi.org/10.1002/cssc.202300936. Acesso em: 16 nov. 2024.
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      Vargas, J. A. M., & Burtoloso, A. C. B. (2023). CO2-Based Carbamate Synthesis Utilizing Reusable Polymer-Supported DBU. ChemSusChem, e202300936. doi:10.1002/cssc.202300936
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      Vargas JAM, Burtoloso ACB. CO2-Based Carbamate Synthesis Utilizing Reusable Polymer-Supported DBU [Internet]. ChemSusChem. 2023 ;e202300936.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/cssc.202300936
    • Vancouver

      Vargas JAM, Burtoloso ACB. CO2-Based Carbamate Synthesis Utilizing Reusable Polymer-Supported DBU [Internet]. ChemSusChem. 2023 ;e202300936.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/cssc.202300936
  • Source: ChemCatChem. Unidade: IQSC

    Subjects: CATÁLISE, IRÍDIO

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      CAIUBY, Clarice Alves Dale et al. Cyclic sulfoxonium ylides: synthesis and chemospecific reactivity in the catalytic alkylation of indoles. ChemCatChem, 2023Tradução . . Disponível em: https://doi.org/10.1002/cctc.202201643. Acesso em: 16 nov. 2024.
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      Caiuby, C. A. D., Vidal, L., Burtoloso, A. C. B., & Aïssa, C. (2023). Cyclic sulfoxonium ylides: synthesis and chemospecific reactivity in the catalytic alkylation of indoles. ChemCatChem. doi:10.1002/cctc.202201643
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      Caiuby CAD, Vidal L, Burtoloso ACB, Aïssa C. Cyclic sulfoxonium ylides: synthesis and chemospecific reactivity in the catalytic alkylation of indoles [Internet]. ChemCatChem. 2023 ;[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/cctc.202201643
    • Vancouver

      Caiuby CAD, Vidal L, Burtoloso ACB, Aïssa C. Cyclic sulfoxonium ylides: synthesis and chemospecific reactivity in the catalytic alkylation of indoles [Internet]. ChemCatChem. 2023 ;[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/cctc.202201643
  • Source: European Journal of Organic Chemistry. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, OXIDAÇÃO, IODO

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      ECHEMENDÍA, Radell et al. Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds. European Journal of Organic Chemistry, v. 2022, n. 26, p. e202200441, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200441. Acesso em: 16 nov. 2024.
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      Echemendía, R., Jesus, M. P. de, Furniel, L. G., Day, D. P., & Burtoloso, A. C. B. (2022). Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds. European Journal of Organic Chemistry, 2022( 26), e202200441. doi:10.1002/ejoc.202200441
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      Echemendía R, Jesus MP de, Furniel LG, Day DP, Burtoloso ACB. Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 26): e202200441.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.202200441
    • Vancouver

      Echemendía R, Jesus MP de, Furniel LG, Day DP, Burtoloso ACB. Molecular iodine mediated oxidation of arylated α- carbonyl sulfoxonium ylides to 1,2-dicarbonyl-containing compounds [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 26): e202200441.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.202200441
  • Source: The Chemical Record. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA

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      DAY, David P e VARGAS, Jorge A. M. e BURTOLOSO, Antonio Carlos Bender. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, v. 21, p. 1-19, 2021Tradução . . Disponível em: https://doi.org/10.1002/tcr.20200017. Acesso em: 16 nov. 2024.
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      Day, D. P., Vargas, J. A. M., & Burtoloso, A. C. B. (2021). Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, 21, 1-19. doi:10.1002/tcr.20200017
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      Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/tcr.20200017
    • Vancouver

      Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/tcr.20200017
  • Source: European Journal of Organic Chemistry. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS

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      VARGAS, Jorge Andrés Mora e DAY, David P e BURTOLOSO, Antonio Carlos Bender. Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, v. press, 2021Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202001132. Acesso em: 16 nov. 2024.
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      Vargas, J. A. M., Day, D. P., & Burtoloso, A. C. B. (2021). Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, press. doi:10.1002/ejoc.202001132
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      Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.202001132
    • Vancouver

      Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.202001132
  • Source: Angewandte Chemie International Edition. Unidade: IQSC

    Subjects: CATÁLISE, REAGENTES

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      MOMO, Patrícia Betoni et al. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides. Angewandte Chemie International Edition, v. 59, p. 15554–15559 , 2020Tradução . . Disponível em: https://doi.org/10.1002/anie.202005563. Acesso em: 16 nov. 2024.
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      Momo, P. B., Leveille, A. N., Farrar, E. H. E., Grayson, M. N., Mattson, A. E., & Burtoloso, A. C. B. (2020). Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides. Angewandte Chemie International Edition, 59, 15554–15559 . doi:10.1002/anie.202005563
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      Momo PB, Leveille AN, Farrar EHE, Grayson MN, Mattson AE, Burtoloso ACB. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides [Internet]. Angewandte Chemie International Edition. 2020 ; 59 15554–15559 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/anie.202005563
    • Vancouver

      Momo PB, Leveille AN, Farrar EHE, Grayson MN, Mattson AE, Burtoloso ACB. Enantioselective S H Insertion Reactions of a-Carbonyl Sulfoxonium Ylides [Internet]. Angewandte Chemie International Edition. 2020 ; 59 15554–15559 .[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/anie.202005563
  • Source: European Journal of Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      SANTOS, Camila S e BURTOLOSO, Antonio Carlos Bender. Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate. European Journal of Organic Chemistry, v. 2018, n. 45, 2018Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201801197. Acesso em: 16 nov. 2024.
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      Santos, C. S., & Burtoloso, A. C. B. (2018). Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate. European Journal of Organic Chemistry, 2018( 45). doi:10.1002/ejoc.201801197
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      Santos CS, Burtoloso ACB. Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 45):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.201801197
    • Vancouver

      Santos CS, Burtoloso ACB. Direct synthesis of highly substituted cyclopentadienes and derivatives from the self-condensation of renewable ethyl levulinate [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 45):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.201801197
  • Source: European Journal of Organic Chemistry. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      SANTIAGO, João Victor e BURTOLOSO, Antonio Carlos Bender. Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones. European Journal of Organic Chemistry, v. 2018, n. 22, p. 2822–2830, 2018Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201800239. Acesso em: 16 nov. 2024.
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      Santiago, J. V., & Burtoloso, A. C. B. (2018). Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones. European Journal of Organic Chemistry, 2018( 22), 2822–2830. doi:10.1002/ejoc.201800239
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      Santiago JV, Burtoloso ACB. Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 22): 2822–2830.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.201800239
    • Vancouver

      Santiago JV, Burtoloso ACB. Rapid synthesis of bicyclic N‐heterocyclic cores from N‐terminal α,β‐unsaturated diazoketones [Internet]. European Journal of Organic Chemistry. 2018 ;2018( 22): 2822–2830.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.201800239
  • Source: ChemistrySelect. Unidade: IQSC

    Assunto: BIOMASSA

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      METZKER, Gustavo e DIAS, Rafael Mafra de Paula e BURTOLOSO, Antonio Carlos Bender. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities. ChemistrySelect, v. 3, n. 2, p. 368-372, 2018Tradução . . Disponível em: https://doi.org/10.1002/slct.201702580. Acesso em: 16 nov. 2024.
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      Metzker, G., Dias, R. M. de P., & Burtoloso, A. C. B. (2018). Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities. ChemistrySelect, 3( 2), 368-372. doi:10.1002/slct.201702580
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      Metzker G, Dias RM de P, Burtoloso ACB. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities [Internet]. ChemistrySelect. 2018 ; 3( 2): 368-372.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/slct.201702580
    • Vancouver

      Metzker G, Dias RM de P, Burtoloso ACB. Iron-catalyzed reductive amination from levulinic and formic acid aqueous solutions: An approach for the selective production of pyrrolidones in biorefinery facilities [Internet]. ChemistrySelect. 2018 ; 3( 2): 368-372.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/slct.201702580
  • Source: Chemistry - A European Journal. Unidade: IQSC

    Assunto: HALOGENAÇÃO

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      GALLO, Rafael D. C et al. Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones. Chemistry - A European Journal, v. 23, p. 16980-16984, 2017Tradução . . Disponível em: https://doi.org/10.1002/chem.201704609. Acesso em: 16 nov. 2024.
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      Gallo, R. D. C., Ahmad, A., Metzker, G., & Burtoloso, A. C. B. (2017). Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones. Chemistry - A European Journal, 23, 16980-16984. doi:10.1002/chem.201704609
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      Gallo RDC, Ahmad A, Metzker G, Burtoloso ACB. Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones [Internet]. Chemistry - A European Journal. 2017 ; 23 16980-16984.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chem.201704609
    • Vancouver

      Gallo RDC, Ahmad A, Metzker G, Burtoloso ACB. Alfa, Alfa-alkylation-halogenation and dihalogenation of sulfoxonium ylides: a direct preparation of geminal difunctionalized ketones [Internet]. Chemistry - A European Journal. 2017 ; 23 16980-16984.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/chem.201704609
  • Source: Synlett. Unidade: IQSC

    Assunto: FOTOQUÍMICA ORGÂNICA

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      TALERO, Alexánder G. e BURTOLOSO, Antonio Carlos Bender. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones. Synlett, v. 28, n. 14, p. 1748-1752, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1590977. Acesso em: 16 nov. 2024.
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      Talero, A. G., & Burtoloso, A. C. B. (2017). Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones. Synlett, 28( 14), 1748-1752. doi:10.1055/s-0036-1590977
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      Talero AG, Burtoloso ACB. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones [Internet]. Synlett. 2017 ; 28( 14): 1748-1752.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/s-0036-1590977
    • Vancouver

      Talero AG, Burtoloso ACB. Sharpless aymmetric dihydroxylation on α,β-unsaturated diazoketones: a new entry for the synthesis of disubstituted furanones [Internet]. Synlett. 2017 ; 28( 14): 1748-1752.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/s-0036-1590977
  • Source: Synthesis. Unidade: IQSC

    Subjects: SÍNTESE ORGÂNICA, UREIA

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      BERNARDIM, Barbara et al. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, v. 48, n. 5, p. 677-686, 2016Tradução . . Disponível em: https://doi.org/10.1055/s-0035-1561061. Acesso em: 16 nov. 2024.
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      Bernardim, B., Couch, E. D., Hardman-Baldwin, A. M., Burtoloso, A. C. B., & Mattson, A. E. (2016). Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, 48( 5), 677-686. doi:10.1055/s-0035-1561061
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      Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/s-0035-1561061
    • Vancouver

      Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1055/s-0035-1561061
  • Source: European Journal of Organic Chemistry. Unidade: IQSC

    Assunto: QUÍMICA ORGÂNICA

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      BURTOLOSO, Antonio Carlos Bender e DIAS, Rafael M e LEONARCZYK, Ives Antonio. Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions. European Journal of Organic Chemistry, n. 23, p. 5005-5016, 2013Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201300581. Acesso em: 16 nov. 2024.
    • APA

      Burtoloso, A. C. B., Dias, R. M., & Leonarczyk, I. A. (2013). Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions. European Journal of Organic Chemistry, ( 23), 5005-5016. doi:10.1002/ejoc.201300581
    • NLM

      Burtoloso ACB, Dias RM, Leonarczyk IA. Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions [Internet]. European Journal of Organic Chemistry. 2013 ;( 23): 5005-5016.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.201300581
    • Vancouver

      Burtoloso ACB, Dias RM, Leonarczyk IA. Sulfoxonium and sulfonium ylides as diazocarbonyl equivalents in metal-catalyzed insertion reactions [Internet]. European Journal of Organic Chemistry. 2013 ;( 23): 5005-5016.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/ejoc.201300581
  • Source: Synthesis. Unidade: IQSC

    Assunto: QUÍMICA ORGÂNICA

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      PRADO, Viviana da Silva e BURTOLOSO, Antonio Carlos Bender. An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid. Synthesis, v. 10, n. 2, p. 361-363, 2010Tradução . . Disponível em: https://www.thieme-connect.com/ejournals/toc/synthesis/99201. Acesso em: 16 nov. 2024.
    • APA

      Prado, V. da S., & Burtoloso, A. C. B. (2010). An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid. Synthesis, 10( 2), 361-363. Recuperado de https://www.thieme-connect.com/ejournals/toc/synthesis/99201
    • NLM

      Prado V da S, Burtoloso ACB. An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid [Internet]. Synthesis. 2010 ; 10( 2): 361-363.[citado 2024 nov. 16 ] Available from: https://www.thieme-connect.com/ejournals/toc/synthesis/99201
    • Vancouver

      Prado V da S, Burtoloso ACB. An improved procedure for the preparation of [bis(2,2,2-trifluoroethyl) phosphono]acetic acid [Internet]. Synthesis. 2010 ; 10( 2): 361-363.[citado 2024 nov. 16 ] Available from: https://www.thieme-connect.com/ejournals/toc/synthesis/99201
  • Source: Synlett. Unidade: IQSC

    Subjects: PRODUTOS NATURAIS, QUÍMICA

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      BURTOLOSO, Antonio Carlos Bender. Catalytic enantioselective 'beta'-arylation of carbonyl compounds. Synlett, n. 2, p. 320-327, 2009Tradução . . Disponível em: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf. Acesso em: 16 nov. 2024.
    • APA

      Burtoloso, A. C. B. (2009). Catalytic enantioselective 'beta'-arylation of carbonyl compounds. Synlett, ( 2), 320-327. Recuperado de http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
    • NLM

      Burtoloso ACB. Catalytic enantioselective 'beta'-arylation of carbonyl compounds [Internet]. Synlett. 2009 ;( 2): 320-327.[citado 2024 nov. 16 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf
    • Vancouver

      Burtoloso ACB. Catalytic enantioselective 'beta'-arylation of carbonyl compounds [Internet]. Synlett. 2009 ;( 2): 320-327.[citado 2024 nov. 16 ] Available from: http://www.thieme-connect.com/ejournals/pdf/synlett/doi/10.1055/s-0028-1087673.pdf

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