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Bifurcated Nickel‐Catalyzed Functionalizations: Heteroarene C−H Activation with Allenes

Nakanowatari, Sachiyo ; Müller, Thomas ; Oliveira, João C. A. ; Ackermann, Lutz

Angewandte Chemie, 2017-12, Vol.129 (50), p.16107-16111 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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  • Título:
    Bifurcated Nickel‐Catalyzed Functionalizations: Heteroarene C−H Activation with Allenes
  • Autor: Nakanowatari, Sachiyo ; Müller, Thomas ; Oliveira, João C. A. ; Ackermann, Lutz
  • Assuntos: Allene ; Bifurcations ; C-H-Aktivierung ; Chemistry ; Heterocyclen ; Imidazole ; Nickel ; Reaktionsmechanismen
  • É parte de: Angewandte Chemie, 2017-12, Vol.129 (50), p.16107-16111
  • Notas: These authors contributed equally to this work.
  • Descrição: A unified strategy for nickel(0)‐catalyzed C−H allylations, alkenylations, and dienylations has been realized through versatile hydroarylations of allenes with ample scope. Thus, an inexpensive nickel catalyst modified with a N‐heterocyclic carbene ligand enabled the direct transformation of C−H bonds of biologically relevant imidazole and purine derivatives with full control of regio‐ and chemoselectivity. Einfache C‐H‐Aktivierung: Gegabelte Nickel(0)‐katalysierte C‐H‐Allylierungen, Alkenylierungen und Dienylierungen wurden durch Hydroarylierung von Allenen unter vollständiger Kontrolle der Regio‐ und Chemoselektivität durchgeführt. Das Substratspektrum umfasst eine Vielzahl von Imidazol‐ und Purinderivaten.
  • Editor: Weinheim: Wiley Subscription Services, Inc
  • Idioma: Inglês;Alemão

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