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Ruthenium(II)-Catalyzed Microwave-Promoted Multiple C-H Activation in Synthesis of Hexa(heteroaryl)benzenes in Water.
Drev, Miha; Groselj, Uros; Ledinek, Bine; Perdih, Franc; Svete, Jurij; Stefane, Bogdan; Pozgan, Franc.
Afiliação
  • Drev M; Faculty of Chemistry and Chemical Technology , University of Ljubljana , Vecna pot 113 , SI-1000 Ljubljana , Slovenia.
  • Groselj U; Faculty of Chemistry and Chemical Technology , University of Ljubljana , Vecna pot 113 , SI-1000 Ljubljana , Slovenia.
  • Ledinek B; Faculty of Chemistry and Chemical Technology , University of Ljubljana , Vecna pot 113 , SI-1000 Ljubljana , Slovenia.
  • Perdih F; Faculty of Chemistry and Chemical Technology , University of Ljubljana , Vecna pot 113 , SI-1000 Ljubljana , Slovenia.
  • Svete J; Faculty of Chemistry and Chemical Technology , University of Ljubljana , Vecna pot 113 , SI-1000 Ljubljana , Slovenia.
  • Stefane B; Faculty of Chemistry and Chemical Technology , University of Ljubljana , Vecna pot 113 , SI-1000 Ljubljana , Slovenia.
  • Pozgan F; Faculty of Chemistry and Chemical Technology , University of Ljubljana , Vecna pot 113 , SI-1000 Ljubljana , Slovenia.
Org Lett ; 20(17): 5268-5273, 2018 09 07.
Article em En | MEDLINE | ID: mdl-30130120
ABSTRACT
A series of hexa(heteroaryl)benzenes were synthesized by the Ru(II)-carboxylate-catalyzed multiple C-H activation of benzenes carrying pyridyl, pyrimidyl, or pyrazolyl directing groups using N-heteroaryl bromides as coupling partners. The reactions proceeded with high selectivity under microwave irradiation in water. Iterative penta-arylation could be implemented via activation of C-H bonds of generated intermediates by cascade chelation assistance of in situ installed pyridyl groups. This strategy provides multidentate ligands for selective complexation of transition metals and potential building of photoredox systems.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article