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Synthesis of N-Fused Polycyclic Indole Derivatives via Ru(II)-Catalyzed C-H Bond Activation and Intramolecular Hydroarylation.
Udayanga, D M Nirosh; Le, Nghia; Schwirian, Elijah N; Donnadieu, Bruno; Nash, Kye; Collier, Willard; Webster, Charles Edwin; Cui, Xin.
Afiliação
  • Udayanga DMN; Department of Chemistry, Mississippi State University, Mississippi State, Mississippi 39762, United States.
  • Le N; Department of Chemistry, Mississippi State University, Mississippi State, Mississippi 39762, United States.
  • Schwirian EN; Department of Chemistry, Mississippi State University, Mississippi State, Mississippi 39762, United States.
  • Donnadieu B; Department of Chemistry, Mississippi State University, Mississippi State, Mississippi 39762, United States.
  • Nash K; Department of Chemistry, Tuskegee University, Tuskegee, Alabama 36088, United States.
  • Collier W; Department of Chemistry, Tuskegee University, Tuskegee, Alabama 36088, United States.
  • Webster CE; Department of Chemistry, Mississippi State University, Mississippi State, Mississippi 39762, United States.
  • Cui X; Department of Chemistry, Mississippi State University, Mississippi State, Mississippi 39762, United States.
Org Lett ; 25(48): 8745-8750, 2023 Dec 08.
Article em En | MEDLINE | ID: mdl-38032145
A new synthesis of N-fused tetracyclic indole derivatives and their related polycyclic analogues has been developed based on ruthenium(II)-catalyzed C-H activation and intramolecular hydroarylation. A series of polycyclic indoles with a 3-formyl group have been prepared in good to high yields. Various aliphatic and aromatic amines have been studied to form a transient directing group with the aldehyde for the catalytic process. A significant impact of the structures of the aromatic amines was identified, and 1-naphthylamine was shown to enable the catalytic process. DFT computations were performed to gain further insight into the role of the transient directing groups.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article