A novel method for the preparation of 4-arylimidazolones.
Org Lett
; 15(11): 2830-3, 2013 Jun 07.
Article
in En
| MEDLINE
| ID: mdl-23713942
ABSTRACT
A series of 4-arylimidazolones have been accessed via late-stage, palladium-mediated arylation of acetone- and cyclohexanone-derived 4-chloroimidazolones. The 4-chloroimidazolones were prepared via a novel rearrangement of the corresponding imidazolone N-oxides. This communication serves as an expansion of chemistry originally developed for our glucagon receptor antagonist program.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Receptors, Glucagon
/
Cyclic N-Oxides
/
Imidazoles
Language:
En
Journal:
Org Lett
Journal subject:
BIOQUIMICA
Year:
2013
Document type:
Article
Affiliation country: