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Catalytic Synthesis of Substituted Indoles and Quinolines from the Dehydrative C-H Coupling of Arylamines with 1,2- and 1,3-Diols. Organometallics 2016 Jun 13;35(11):1973-1977

Date

06/13/2016

Pubmed ID

30505062

Pubmed Central ID

PMC6261509

DOI

10.1021/acs.organomet.6b00273

Scopus ID

2-s2.0-84974784214 (requires institutional sign-in at Scopus site)   28 Citations

Abstract

The cationic ruthenium-hydride complex catalyzes dehydrative C-H coupling reaction of arylamines with 1,2-diols to form the indole products. The analogous coupling of arylamines with 1,3-diols afforded the substituted quinolines. The catalytic method directly forms these coupling products in a highly regioselective manner without generating any toxic byproducts.

Author List

Lee H, Yi CS

Author

Chae Yi PhD Professor, Inorganic and Organometallic Chemistry, Homogeneous Catalysis in the Chemistry department at Marquette University