Tandem-type Pd(II)-catalyzed oxidative Heck reaction/intramolecular C-H amidation sequence: a novel route to 4-aryl-2-quinolinones.
Kiyofumi Inamoto, Junpei Kawasaki, Kou Hiroya, Yoshinori Kondo, Takayuki Doi
Index: Chem. Commun. (Camb.) 36th ed., 48 , 4332-4334, (2012)
Full Text: HTML
Abstract
A novel catalytic method for synthesizing 4-aryl-2-quinolinones is reported. The process involves two mechanistically independent, sequential Pd(II)-catalyzed reactions--the oxidative Heck reaction and the intramolecular C-H amidation--both of which smoothly proceed in the presence of a single catalytic system in a one-pot manner.
Related Compounds
Related Articles:
Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.
2012-04-06
[Org. Lett. 7th ed., 14 , 1930-1933, (2012)]
2012-05-01
[Magn. Reson. Chem. 5th ed., 50 , 379-387, (2012)]
2006-12-08
[J. Org. Chem. 71 , 9522, (2006)]
Synthesis of terphenyl benzimidazoles as tubulin polymerization inhibitors.
2012-04-01
[Eur. J. Med. Chem. 50 , 9-17, (2012)]
2012-04-21
[Org. Biomol. Chem. 15th ed., 10 , 2955-2959, (2012)]