LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Synthesis of Dibenzo[ f , h ]quinolines by Stepwise C–H Arylation of 2-Phenylpyridine and Reductive Cyclodehydrogenation

Photo by nextdistro from unsplash

A synthetic approach to dibenzo[f,h]quinolines and their derivatives is presented via stepwise ruthenium-catalyzed C-H arylation and potassium-mediated reductive cyclodehydrogenation from 2-phenylpyridine and aryl bromides. One dibenzo[f,h]quinoline derivative is used as… Click to show full abstract

A synthetic approach to dibenzo[f,h]quinolines and their derivatives is presented via stepwise ruthenium-catalyzed C-H arylation and potassium-mediated reductive cyclodehydrogenation from 2-phenylpyridine and aryl bromides. One dibenzo[f,h]quinoline derivative is used as a bidentate ligand to prepare a cyclometalated ruthenium complex. Two dibenzo[f,h]quinoline compounds and the ruthenium complex are characterized by single-crystal X-ray structural analysis.

Keywords: phenylpyridine; dibenzo; reductive cyclodehydrogenation; arylation; dibenzo quinolines

Journal Title: Synthesis
Year Published: 2023

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.