1.
Org Lett
; 6(25): 4759-62, 2004 Dec 09.
Artículo
en Inglés
| MEDLINE
| ID: mdl-15575679
RESUMEN
[reaction: see text] 6-Phenanthridinones and their heterocyclic analogues were synthesized through a one-pot procedure based on consecutive Pd-catalyzed aryl-aryl and N-aryl coupling from iodoarenes ortho-substituted by electron-releasing substituents and amides of o-bromoarene- and heteroarenecarboxylic acids.