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Filtros : "Chemistry European Journal" Limpar

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  • Artigo de periodico

    Electron-induced reactions in 3-bromopyruvic acid (2019)

    Silva, Filipe Ferreira da; Varella, Márcio Teixeira do Nascimento; Jones, Nykola C; Hoffmann, Søren Vrønning; Denifl, Stephan; Bald, Ilko; Kopyra, Janina

    Source: Chemistry European Journal. Unidade: IF

    Assunto: ELÉTRONS

    PrivadoAcesso à fonteDOIHow to cite
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    • ABNT

      SILVA, Filipe Ferreira da et al. Electron-induced reactions in 3-bromopyruvic acid. Chemistry European Journal, v. 25, p. 5498–5506, 2019Tradução . . Disponível em: https://doi.org/10.1002/chem.201806132. Acesso em: 01 jun. 2024.

    • APA

      Silva, F. F. da, Varella, M. T. do N., Jones, N. C., Hoffmann, S. V., Denifl, S., Bald, I., & Kopyra, J. (2019). Electron-induced reactions in 3-bromopyruvic acid. Chemistry European Journal, 25, 5498–5506. doi:10.1002/chem.201806132

    • NLM

      Silva FF da, Varella MT do N, Jones NC, Hoffmann SV, Denifl S, Bald I, Kopyra J. Electron-induced reactions in 3-bromopyruvic acid [Internet]. Chemistry European Journal. 2019 ;25 5498–5506.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/chem.201806132

    • Vancouver

      Silva FF da, Varella MT do N, Jones NC, Hoffmann SV, Denifl S, Bald I, Kopyra J. Electron-induced reactions in 3-bromopyruvic acid [Internet]. Chemistry European Journal. 2019 ;25 5498–5506.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/chem.201806132

  • Artigo de periodico

    Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins (2018)

    Oliveira, Juliana Manso de; Angnes, Ricardo Almir; Khan, Ismat Ullah; Polo, Ellen Christine; Heerdt, Gabriel; Servilha, Bruno M; Silva, Vitor H. Menezes da; Braga, Ataualpa Albert Carmo ; Correia, Carlos Roque Duarte

    Source: Chemistry European Journal. Unidade: IQ

    Subjects: CATÁLISE, PALÁDIO

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    • ABNT

      OLIVEIRA, Juliana Manso de et al. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, v. 24, n. 45, p. 11738-11747, 2018Tradução . . Disponível em: https://doi.org/10.1002/chem.201801910. Acesso em: 01 jun. 2024.

    • APA

      Oliveira, J. M. de, Angnes, R. A., Khan, I. U., Polo, E. C., Heerdt, G., Servilha, B. M., et al. (2018). Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins. Chemistry European Journal, 24( 45), 11738-11747. doi:10.1002/chem.201801910

    • NLM

      Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/chem.201801910

    • Vancouver

      Oliveira JM de, Angnes RA, Khan IU, Polo EC, Heerdt G, Servilha BM, Silva VHM da, Braga AAC, Correia CRD. Enantioselective non-covalent substrate directable Heck-Matsuda and oxidative Heck arylations of unactivated five-membered carbocyclic olefins [Internet]. Chemistry European Journal. 2018 ; 24( 45): 11738-11747.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/chem.201801910
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