Filtros : "Darbem, Mariana P" "Pimenta, Daniel Carvalho" Removido: "Eliaschewitz, Freddy Goldberg" Limpar

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  • Source: RSC Advances. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA

    Versão PublicadaAcesso à fonteDOIHow to cite
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    • ABNT

      DARBEM, Mariana P et al. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, v. 12, p. 2145–2149, 2022Tradução . . Disponível em: https://doi.org/10.1039/d1ra08388k. Acesso em: 07 nov. 2024.
    • APA

      Darbem, M. P., Esteves, H. A., Burrow, R. A., Paulino, A. A. S., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, 12, 2145–2149. doi:10.1039/d1ra08388k
    • NLM

      Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1039/d1ra08388k
    • Vancouver

      Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1039/d1ra08388k
  • Source: ChemCatChem. Unidades: BIOTECNOLOGIA, FCF, IQ

    Subjects: PALÁDIO, HIDRÓLISE

    Acesso à fonteDOIHow to cite
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    • ABNT

      DARBEM, Mariana P et al. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, v. 12, n. 2, p. 576-583, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.201901403. Acesso em: 07 nov. 2024.
    • APA

      Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, Pimenta, D. C., & Stefani, H. A. (2020). Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, 12( 2), 576-583. doi:10.1002/cctc.201901403
    • NLM

      Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/cctc.201901403
    • Vancouver

      Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/cctc.201901403
  • Source: European Journal of Organic Chemistry. Unidades: BIOTECNOLOGIA, FCF

    Subjects: MONÓXIDO DE CARBONO, PALÁDIO

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    • ABNT

      ESTEVES, Henrique A et al. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, v. 2019, p. 7384-7388, 2019Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201901081. Acesso em: 07 nov. 2024.
    • APA

      Esteves, H. A., Darbem, M. P., Pimenta, D. C., & Stefani, H. A. (2019). Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides. European Journal of Organic Chemistry, 2019, 7384-7388. doi:10.1002/ejoc.201901081
    • NLM

      Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ejoc.201901081
    • Vancouver

      Esteves HA, Darbem MP, Pimenta DC, Stefani HA. Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides [Internet]. European Journal of Organic Chemistry. 2019 ; 2019 7384-7388.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/ejoc.201901081
  • Source: Advanced Synthesis and Catalysis. Unidade: FCF

    Subjects: CALCOGÊNIOS, COMPOSTOS HETEROCÍCLICOS, FERRO

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    • ABNT

      OLIVEIRA, Isadora M. de et al. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, v. 361, n. 13, p. 3163-3172, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900142. Acesso em: 07 nov. 2024.
    • APA

      Oliveira, I. M. de, Esteves, C. H. A., Darbem, M. P., Pimenta, D. C., Schpector, J. Z., Ferreira, A. G., et al. (2019). Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization. Advanced Synthesis and Catalysis, 361( 13), 3163-3172. doi:10.1002/adsc.201900142
    • NLM

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/adsc.201900142
    • Vancouver

      Oliveira IM de, Esteves CHA, Darbem MP, Pimenta DC, Schpector JZ, Ferreira AG, Stefani HA, Manarin F. Iron (III)-Promoted synthesis of substituted 4H-Chalcogenochromenes and chemoselective functionalization [Internet]. Advanced Synthesis and Catalysis. 2019 ; 361( 13): 3163-3172.[citado 2024 nov. 07 ] Available from: https://doi.org/10.1002/adsc.201900142

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