37867-75-7Relevant articles and documents
Metal-free nitrogenation of 2-acetylbiphenyls: Expeditious synthesis of phenanthridines
Tang, Conghui,Yuan, Yizhi,Jiao, Ning
supporting information, p. 2206 - 2209 (2015/05/13)
An intermolecular nitrogenation reaction toward the synthesis of phenanthridines has been developed. This metal-free protocol provides a novel nitrogen-incorporation transformation using azides as the nitrogen source. Phenanthridines, which are of great interest in pharmaceutical and medicinal chemistry, are synthesized efficiently in one step. Moreover, the byproducts derived from the Schmidt reaction are inhibited, which further demonstrated the high chemoselectivity of this transformation.
Palladium and radical routes to phenanthridines
Bowman, W. Russell,Lyon, Jessica E.,Pritchard, Gareth J.
, p. 210 - 227 (2013/01/16)
Two routes to phenanthridines are reported; a palladium-mediated route using imidoyl-selanides as precursors and a modified radical route using aryl imines as starting materials. ARKAT-USA, Inc.
Convergent synthesis of 6-substituted phenanthridines via anionic ring closure
Lysen, Morten,Kristensen, Jesper L.,Vedso, Per,Begtrup, Mikael
, p. 257 - 259 (2007/10/03)
Chemical equation presented The addition of organometallic derivatives to the cyano group of 2-(2-fluorophenyl)benzonitrile followed by intramolecular nucleophilic substitution produces 6-substituted phenanthridines. Alkyllithiums, aryllithiums, and steri
