Filtros : "QUÍMICA ORGÂNICA" "Alemanha" Removido: "HU" Limpar

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  • 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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1002/chem.202400108
  • Source: Energy Technology. Unidade: IQSC

    Subjects: GÁS CARBÔNICO, ELETROQUÍMICA, QUÍMICA ORGÂNICA

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      REIS, Eduardo Arizono dos et al. Revisiting electrocatalytic CO2 reduction in non aqueous media: promoting CO2 recycling in organic molecules by controlling H2 evolution. Energy Technology, p. 2201367, 2023Tradução . . Disponível em: https://doi.org/10.1002/ente.202201367. Acesso em: 02 nov. 2024.
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      Reis, E. A. dos, Silva, G. T. S. T. da, Santiago, E. I., & Ribeiro, C. (2023). Revisiting electrocatalytic CO2 reduction in non aqueous media: promoting CO2 recycling in organic molecules by controlling H2 evolution. Energy Technology, 2201367. doi:10.1002/ente.202201367
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      Reis EA dos, Silva GTST da, Santiago EI, Ribeiro C. Revisiting electrocatalytic CO2 reduction in non aqueous media: promoting CO2 recycling in organic molecules by controlling H2 evolution [Internet]. Energy Technology. 2023 ;2201367.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ente.202201367
    • Vancouver

      Reis EA dos, Silva GTST da, Santiago EI, Ribeiro C. Revisiting electrocatalytic CO2 reduction in non aqueous media: promoting CO2 recycling in organic molecules by controlling H2 evolution [Internet]. Energy Technology. 2023 ;2201367.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ente.202201367
  • 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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1002/ejoc.202200441
  • Source: ChemistrySelect. Unidade: IQ

    Subjects: DOENÇAS INFECCIOSAS, MALÁRIA, SAIS, QUÍMICA ORGÂNICA, QUÍMICA SUPRAMOLECULAR

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      ALI, Akbar et al. Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids. ChemistrySelect, v. 7, p. 1-13 art. e202200349, 2022Tradução . . Disponível em: https://doi.org/10.1002/slct.202200349. Acesso em: 02 nov. 2024.
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      Ali, A., Khalid, M., Ashfaq, M., Malik, A. N., Muhammad Nawaz Tahir,, Assiri, M. A., et al. (2022). Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids. ChemistrySelect, 7, 1-13 art. e202200349. doi:10.1002/slct.202200349
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      Ali A, Khalid M, Ashfaq M, Malik AN, Muhammad Nawaz Tahir, Assiri MA, Imran M, Morais SF de A, Braga AAC. Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids [Internet]. ChemistrySelect. 2022 ; 7 1-13 art. e202200349.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/slct.202200349
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      Ali A, Khalid M, Ashfaq M, Malik AN, Muhammad Nawaz Tahir, Assiri MA, Imran M, Morais SF de A, Braga AAC. Preparation, QTAIM and single-crystal exploration of the Pyrimethamine-based co-crystal salts with substituted benzoic acids [Internet]. ChemistrySelect. 2022 ; 7 1-13 art. e202200349.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/slct.202200349
  • 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: 02 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. 02 ] 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. 02 ] 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: 02 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. 02 ] Available from: https://doi.org/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. 02 ] Available from: https://doi.org/10.1002/ejoc.202001132
  • Source: European Journal of Organic Chemistry. Unidade: FCFRP

    Subjects: QUÍMICA ORGÂNICA, BIOMASSA, CARBOIDRATOS, GLICOSE

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      SANTOS, Thiago dos et al. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, v. 2020, n. 41, p. 6429-6432, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000970. Acesso em: 02 nov. 2024.
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      Santos, T. dos, Grundke, C., Lucas, T., Großmann, L., Clososki, G. C., & Opatz, T. (2020). Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, 2020( 41), 6429-6432. doi:10.1002/ejoc.202000970
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      Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ejoc.202000970
    • Vancouver

      Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ejoc.202000970
  • Source: ChemistrySelect. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, CATALISADORES

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      ZANIN, Lucas Lima e PORTO, Andre Luiz Meleiro. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, v. 5, n. 28, p. 8604-8608, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202001830. Acesso em: 02 nov. 2024.
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      Zanin, L. L., & Porto, A. L. M. (2020). HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, 5( 28), 8604-8608. doi:10.1002/slct.202001830
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      Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/slct.202001830
    • Vancouver

      Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/slct.202001830
  • Source: Abstracts. Conference titles: EPNOE 2017 - International Polysaccharide Conference. Unidade: IQSC

    Subjects: QUÍMICA ORGÂNICA, BIOMASSA

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      SANTOS, Rachel Passos de Oliveira et al. Lignocellulosic biomass as a source of materials and fermentable sugars. 2017, Anais.. Jena: Instituto de Química de São Carlos, Universidade de São Paulo, 2017. Disponível em: http://www.epnoe2017.de/fileadmin/congress/media/epnoe2017/druckelemente/EPNOE2017_Abstractband.pdf. Acesso em: 02 nov. 2024.
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      Santos, R. P. de O., Rossi, P., Ferracini, T. V., Kaschuk, J. J., Gomes, B. L., Catunda, L., & Frollini, E. (2017). Lignocellulosic biomass as a source of materials and fermentable sugars. In Abstracts. Jena: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de http://www.epnoe2017.de/fileadmin/congress/media/epnoe2017/druckelemente/EPNOE2017_Abstractband.pdf
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      Santos RP de O, Rossi P, Ferracini TV, Kaschuk JJ, Gomes BL, Catunda L, Frollini E. Lignocellulosic biomass as a source of materials and fermentable sugars [Internet]. Abstracts. 2017 ;[citado 2024 nov. 02 ] Available from: http://www.epnoe2017.de/fileadmin/congress/media/epnoe2017/druckelemente/EPNOE2017_Abstractband.pdf
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      Santos RP de O, Rossi P, Ferracini TV, Kaschuk JJ, Gomes BL, Catunda L, Frollini E. Lignocellulosic biomass as a source of materials and fermentable sugars [Internet]. Abstracts. 2017 ;[citado 2024 nov. 02 ] Available from: http://www.epnoe2017.de/fileadmin/congress/media/epnoe2017/druckelemente/EPNOE2017_Abstractband.pdf
  • Source: Chemistry: a European Journal. Unidade: IFSC

    Subjects: RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA, NANOPARTÍCULAS, QUÍMICA ORGÂNICA, SILÍCIO

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      SURMIAK, Sabrina K. et al. Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions. Chemistry: a European Journal, v. 23, n. 25, p. 6019-6028, 2017Tradução . . Disponível em: https://doi.org/10.1002/chem.201604508. Acesso em: 02 nov. 2024.
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      Surmiak, S. K., Doerenkamp, C., Selter, P., Peterlechner, M., Schäfer, A. H., Eckert, H., & Studer, A. (2017). Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions. Chemistry: a European Journal, 23( 25), 6019-6028. doi:10.1002/chem.201604508
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      Surmiak SK, Doerenkamp C, Selter P, Peterlechner M, Schäfer AH, Eckert H, Studer A. Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6019-6028.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/chem.201604508
    • Vancouver

      Surmiak SK, Doerenkamp C, Selter P, Peterlechner M, Schäfer AH, Eckert H, Studer A. Palladium nanoparticle loaded bifunctional silica hybrid material: preparation and applications as catalyst in hydrogenation reactions [Internet]. Chemistry: a European Journal. 2017 ; 23( 25): 6019-6028.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/chem.201604508
  • Source: European Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP

    Subjects: QUÍMICA ORGÂNICA, MAGNÉSIO, SÍNTESE ORGÂNICA

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      BATISTA, João H. C. et al. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl. European Journal of Organic Chemistry, v. 2015, n. 5, p. 967-977, 2015Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201403255. Acesso em: 02 nov. 2024.
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      Batista, J. H. C., Santos, F. M. dos, Bozzini, L. A., Vessecchi, R., Oliveira, A. R. M. de, & Clososki, G. C. (2015). Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl. European Journal of Organic Chemistry, 2015( 5), 967-977. doi:10.1002/ejoc.201403255
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      Batista JHC, Santos FM dos, Bozzini LA, Vessecchi R, Oliveira ARM de, Clososki GC. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl [Internet]. European Journal of Organic Chemistry. 2015 ; 2015( 5): 967-977.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ejoc.201403255
    • Vancouver

      Batista JHC, Santos FM dos, Bozzini LA, Vessecchi R, Oliveira ARM de, Clososki GC. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl [Internet]. European Journal of Organic Chemistry. 2015 ; 2015( 5): 967-977.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ejoc.201403255
  • Source: Frustrated Lewis Pairs I. Unidade: IFSC

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, ESPECTROSCOPIA, QUÍMICA ORGÂNICA

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      WIEGAND, Thomas e HELLMUT ECKERT, e GRIMME, Stefan. Solid-state NMR as a spectroscopic tool for characterizing phosphane-borane frustrated lewis pairs. Frustrated Lewis Pairs I. Tradução . Heidelberg: Springer, 2013. . Disponível em: https://doi.org/10.1007/128_2012_386. Acesso em: 02 nov. 2024.
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      Wiegand, T., Hellmut Eckert,, & Grimme, S. (2013). Solid-state NMR as a spectroscopic tool for characterizing phosphane-borane frustrated lewis pairs. In Frustrated Lewis Pairs I. Heidelberg: Springer. doi:10.1007/128_2012_386
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      Wiegand T, Hellmut Eckert, Grimme S. Solid-state NMR as a spectroscopic tool for characterizing phosphane-borane frustrated lewis pairs [Internet]. In: Frustrated Lewis Pairs I. Heidelberg: Springer; 2013. [citado 2024 nov. 02 ] Available from: https://doi.org/10.1007/128_2012_386
    • Vancouver

      Wiegand T, Hellmut Eckert, Grimme S. Solid-state NMR as a spectroscopic tool for characterizing phosphane-borane frustrated lewis pairs [Internet]. In: Frustrated Lewis Pairs I. Heidelberg: Springer; 2013. [citado 2024 nov. 02 ] Available from: https://doi.org/10.1007/128_2012_386
  • Source: Angewandte Chemie. Unidades: FMRP, FORP, IQ, FCFRP

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA, CARAMBOLA (TOXICIDADE)

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      GARCIA-CAIRASCO, Norberto et al. Elucidating the neurotoxicity of the star fruit. Angewandte Chemie, v. 52, p. 13067-13070, 2013Tradução . . Disponível em: https://doi.org/10.1002/anie.201305382. Acesso em: 02 nov. 2024.
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      Garcia-Cairasco, N., Moyses Neto, M., Del Vecchio, F., Oliveira, J. A. C., Santos, F. L. dos, Castro, O. W. de, et al. (2013). Elucidating the neurotoxicity of the star fruit. Angewandte Chemie, 52, 13067-13070. doi:10.1002/anie.201305382
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      Garcia-Cairasco N, Moyses Neto M, Del Vecchio F, Oliveira JAC, Santos FL dos, Castro OW de, Arisi GM, Dantas M, Carolino ROG, Coutinho Netto J, Dagostin ALA, Rodrigues MCA, Leão RMX, Quintiliano SAP, Silva Junior LF da, Gobbo Neto L, Lopes NP. Elucidating the neurotoxicity of the star fruit [Internet]. Angewandte Chemie. 2013 ; 52 13067-13070.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/anie.201305382
    • Vancouver

      Garcia-Cairasco N, Moyses Neto M, Del Vecchio F, Oliveira JAC, Santos FL dos, Castro OW de, Arisi GM, Dantas M, Carolino ROG, Coutinho Netto J, Dagostin ALA, Rodrigues MCA, Leão RMX, Quintiliano SAP, Silva Junior LF da, Gobbo Neto L, Lopes NP. Elucidating the neurotoxicity of the star fruit [Internet]. Angewandte Chemie. 2013 ; 52 13067-13070.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/anie.201305382
  • Source: Angewandte Chemie. Unidades: FMRP, FORP, IQ, FCFRP

    Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA, CARAMBOLA (TOXICIDADE)

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      CAIRASCO, Norberto Garcia et al. Elucidating the neurotoxicity of the star fruit. Angewandte Chemie, v. 125, n. 49, p. 13305-13308, 2013Tradução . . Disponível em: https://doi.org/10.1002/ange.201305382. Acesso em: 02 nov. 2024.
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      Cairasco, N. G., Moyses Neto, M., Del Vecchio, F., Oliveira, J. A. C., Santos, F. L. dos, Castro, O. W. de, et al. (2013). Elucidating the neurotoxicity of the star fruit. Angewandte Chemie, 125( 49), 13305-13308. doi:10.1002/ange.201305382
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      Cairasco NG, Moyses Neto M, Del Vecchio F, Oliveira JAC, Santos FL dos, Castro OW de, Arisi GM, Dantas M, Carolino R de OG, Coutinho Netto J, Dagostin ALA, Rodrigues MCA, Leão RM, Quintiliano SAP, Silva Junior LF da, Gobbo Neto L, Lopes NP. Elucidating the neurotoxicity of the star fruit [Internet]. Angewandte Chemie. 2013 ; 125( 49): 13305-13308.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ange.201305382
    • Vancouver

      Cairasco NG, Moyses Neto M, Del Vecchio F, Oliveira JAC, Santos FL dos, Castro OW de, Arisi GM, Dantas M, Carolino R de OG, Coutinho Netto J, Dagostin ALA, Rodrigues MCA, Leão RM, Quintiliano SAP, Silva Junior LF da, Gobbo Neto L, Lopes NP. Elucidating the neurotoxicity of the star fruit [Internet]. Angewandte Chemie. 2013 ; 125( 49): 13305-13308.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/ange.201305382
  • 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: 02 nov. 2024.
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      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. 02 ] 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. 02 ] Available from: https://doi.org/10.1002/ejoc.201300581
  • Source: Organoselenium Chemistry. Unidade: IQ

    Subjects: SELÊNIO, QUÍMICA ORGÂNICA

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      COMASSETO, João Valdir e SANTOS, Alcindo Aparecido dos e WENDLER, Edison P. Selenium-stabilized carbanions. Organoselenium Chemistry. Tradução . Weinheim: Wiley-VCH, 2012. . . Acesso em: 02 nov. 2024.
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      Comasseto, J. V., Santos, A. A. dos, & Wendler, E. P. (2012). Selenium-stabilized carbanions. In Organoselenium Chemistry. Weinheim: Wiley-VCH.
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      Comasseto JV, Santos AA dos, Wendler EP. Selenium-stabilized carbanions. In: Organoselenium Chemistry. Weinheim: Wiley-VCH; 2012. [citado 2024 nov. 02 ]
    • Vancouver

      Comasseto JV, Santos AA dos, Wendler EP. Selenium-stabilized carbanions. In: Organoselenium Chemistry. Weinheim: Wiley-VCH; 2012. [citado 2024 nov. 02 ]
  • Source: Journal of Separation Science. Unidade: FCFRP

    Subjects: QUÍMICA ORGÂNICA, METABÓLITOS, BIOTRANSFORMAÇÃO

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      CALIXTO, Leandro Augusto e BONATO, Pierina Sueli. Simultaneous determination of rosiglitazone and its metabolites in rat liver microsomal fraction using hollow-fiber liquid-phase microextraction for sample preparation. Journal of Separation Science, v. 33, n. 17-18, p. 2872-2880, 2010Tradução . . Disponível em: https://doi.org/10.1002/jssc.201000380. Acesso em: 02 nov. 2024.
    • APA

      Calixto, L. A., & Bonato, P. S. (2010). Simultaneous determination of rosiglitazone and its metabolites in rat liver microsomal fraction using hollow-fiber liquid-phase microextraction for sample preparation. Journal of Separation Science, 33( 17-18), 2872-2880. doi:10.1002/jssc.201000380
    • NLM

      Calixto LA, Bonato PS. Simultaneous determination of rosiglitazone and its metabolites in rat liver microsomal fraction using hollow-fiber liquid-phase microextraction for sample preparation [Internet]. Journal of Separation Science. 2010 ; 33( 17-18): 2872-2880.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/jssc.201000380
    • Vancouver

      Calixto LA, Bonato PS. Simultaneous determination of rosiglitazone and its metabolites in rat liver microsomal fraction using hollow-fiber liquid-phase microextraction for sample preparation [Internet]. Journal of Separation Science. 2010 ; 33( 17-18): 2872-2880.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/jssc.201000380
  • 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: 02 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. 02 ] 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. 02 ] Available from: https://www.thieme-connect.com/ejournals/toc/synthesis/99201
  • Source: Helvetica Chimica Acta. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS

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      ALMEIDA-LAFETÁ, Rita C et al. Withanolides from Aureliana fasciculata var. fasciculata. Helvetica Chimica Acta, v. 93, n. 12, p. 2478-2487, 2010Tradução . . Disponível em: https://doi.org/10.1002/hlca.201000126. Acesso em: 02 nov. 2024.
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      Almeida-Lafetá, R. C., Ferreira, M. J. P., Emerenciano, V. de P., & Kaplan, M. A. C. (2010). Withanolides from Aureliana fasciculata var. fasciculata. Helvetica Chimica Acta, 93( 12), 2478-2487. doi:10.1002/hlca.201000126
    • NLM

      Almeida-Lafetá RC, Ferreira MJP, Emerenciano V de P, Kaplan MAC. Withanolides from Aureliana fasciculata var. fasciculata [Internet]. Helvetica Chimica Acta. 2010 ; 93( 12): 2478-2487.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/hlca.201000126
    • Vancouver

      Almeida-Lafetá RC, Ferreira MJP, Emerenciano V de P, Kaplan MAC. Withanolides from Aureliana fasciculata var. fasciculata [Internet]. Helvetica Chimica Acta. 2010 ; 93( 12): 2478-2487.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1002/hlca.201000126
  • Source: Zeitschrift für Naturforschung B. Unidade: IFSC

    Subjects: MOLÉCULA (ESTRUTURA), DIFRAÇÃO POR RAIOS X, QUÍMICA ORGÂNICA

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      CASTELLANO, Eduardo Ernesto et al. Two new supramolecular assemblies obtained by reaction between saccharin and long-chain diamines. Zeitschrift für Naturforschung B, v. 64, n. 9, p. 1041-1045, 2009Tradução . . Disponível em: https://doi.org/10.1515/znb-2009-0908. Acesso em: 02 nov. 2024.
    • APA

      Castellano, E. E., Piro, O. E., Costa, B. S. P., & Baran, E. J. (2009). Two new supramolecular assemblies obtained by reaction between saccharin and long-chain diamines. Zeitschrift für Naturforschung B, 64( 9), 1041-1045. doi:10.1515/znb-2009-0908
    • NLM

      Castellano EE, Piro OE, Costa BSP, Baran EJ. Two new supramolecular assemblies obtained by reaction between saccharin and long-chain diamines [Internet]. Zeitschrift für Naturforschung B. 2009 ; 64( 9): 1041-1045.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1515/znb-2009-0908
    • Vancouver

      Castellano EE, Piro OE, Costa BSP, Baran EJ. Two new supramolecular assemblies obtained by reaction between saccharin and long-chain diamines [Internet]. Zeitschrift für Naturforschung B. 2009 ; 64( 9): 1041-1045.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1515/znb-2009-0908

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