107209-63-2Relevant articles and documents
Synthesis of 6-aroyl phenanthridines by Fe-catalyzed oxidative radical cyclization of 2-isocyanobiphenyls with benzylic alcohols
Nie, Ziyi,Ding, Qiuping,Peng, Yiyuan
, p. 8350 - 8357 (2016)
A practical method for the synthesis of 6-aroyl phenanthridine derivatives by Fe-catalyzed oxidative radical cyclization of 2-isocyanobiphenyls with benzylic alcohols is described. In addition, this cyclization could be occurred by using toluene as aroyl source. The procedure tolerates various functional groups under simple conditions. A single-electron-transfer pathway is proposed according to mechanistic studies.
Cycloaddition Reactions of Ketoimines. Part II. Synthesis of Substituted Phenanthridines and Cyclopentaquinolines
Lucchini, Vittorio,Prato, Maurizio,Scorrano, Giafranco,Tecilla, Paolo
, p. 1135 - 1139 (2007/10/02)
Substituted 4-benzoyl-3a,4,5,9b-tetrahydro-3H-cyclopentaquinolines 3 and 6-benzoyl-5,6,6a,7,8,10a-hexahydrophenanthridines 10 are obtained through Lewis acid catalyzed addition of 1-phenyl-2-arylamino-2-methoxyethanones 2 to cyclopentadienes and 1,3-cy