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Filtros : "Chemistry European Journal" Limpar

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  • Artigo de periodico

    Gold promoted biocompatible selenium arylation of small molecules, peptides and proteins (2024)

    Nakahata, Douglas H ; Kanavos, Ioannis; Ulacia, Maria Zubiria; Inague, Alex ; Salassa, Luca ; Lobinski, Ryszard; Miyamoto, Sayuri ; Matxain, Jon Mattin; Ronga, Luisa; Paiva, Raphael E. F. de

    Source: Chemistry European Journal. Unidade: IQ

    Subjects: SELÊNIO, PEPTÍDEOS, PROTEÍNAS, OURO

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    • ABNT

      NAKAHATA, Douglas H et al. Gold promoted biocompatible selenium arylation of small molecules, peptides and proteins. Chemistry European Journal, v. 30, n. 15, p. 1-9 art. e202304050, 2024Tradução . . Disponível em: https://dx.doi.org/10.1002/chem.202304050. Acesso em: 11 nov. 2024.

    • APA

      Nakahata, D. H., Kanavos, I., Ulacia, M. Z., Inague, A., Salassa, L., Lobinski, R., et al. (2024). Gold promoted biocompatible selenium arylation of small molecules, peptides and proteins. Chemistry European Journal, 30( 15), 1-9 art. e202304050. doi:10.1002/chem.202304050

    • NLM

      Nakahata DH, Kanavos I, Ulacia MZ, Inague A, Salassa L, Lobinski R, Miyamoto S, Matxain JM, Ronga L, Paiva REF de. Gold promoted biocompatible selenium arylation of small molecules, peptides and proteins [Internet]. Chemistry European Journal. 2024 ; 30( 15): 1-9 art. e202304050.[citado 2024 nov. 11 ] Available from: https://dx.doi.org/10.1002/chem.202304050

    • Vancouver

      Nakahata DH, Kanavos I, Ulacia MZ, Inague A, Salassa L, Lobinski R, Miyamoto S, Matxain JM, Ronga L, Paiva REF de. Gold promoted biocompatible selenium arylation of small molecules, peptides and proteins [Internet]. Chemistry European Journal. 2024 ; 30( 15): 1-9 art. e202304050.[citado 2024 nov. 11 ] Available from: https://dx.doi.org/10.1002/chem.202304050

  • 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

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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: 11 nov. 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 nov. 11 ] 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 nov. 11 ] 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: 11 nov. 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 nov. 11 ] 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 nov. 11 ] Available from: https://doi.org/10.1002/chem.201801910
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