Journal of Organic Chemistry 2007-04-27

Ionic-liquid-promoted palladium-catalyzed multicomponent cyclocarbonylation of o-iodoanilines and allenes to form methylene-2,3-dihydro-1H-quinolin-4-ones.

Fangguo Ye, Howard Alper

Index: J. Org. Chem. 72(9) , 3218-22, (2007)

Full Text: HTML

Abstract

The palladium-catalyzed cyclocarbonylation reaction of o-iodoanilines with allenes and CO in 1-butyl-3-methylimidazolium hexafluorophosphate afforded 3-methylene-2,3-dihydro-1H-quinolin-4-ones in moderate to excellent yields under a low pressure (5 atm) of CO. The ionic liquid, as the solvent and promoter, enhances the efficiency of the cyclocarbonylation reaction. The recyclability of the system of ionic liquid/catalyst/ligand was also demonstrated.


Related Compounds

Related Articles:

Photoinduced intermolecular cross-linking of gas phase triacylglycerol lipid ions.

2015-01-01

[Eur. J. Mass Spectrom. (Chichester, Eng.) 21 , 287-96, (2015)]

Copper-catalyzed three-component synthesis of benzothiazolethiones from o-iodoanilines, isocyanide, and potassium sulfide.

2015-01-02

[Org. Lett. 17(1) , 34-7, (2015)]

Concise synthesis of (+/-)-horsfiline and (+/-)-coerulescine by tandem cyclisation of iodoaryl alkenyl azides.

2003-01-07

[Org. Biomol. Chem. 1(1) , 117-22, (2003)]

Application of ynamides in the synthesis of 2-amidoindoles.

2009-01-01

[Org. Lett. 11(1) , 221-4, (2009)]

m-[125I]iodoaniline: a useful reagent for radiolabeling biotin.

1992-04-01

[Int. J. Rad. Appl. Instrum. B 19(3) , 297-301, (1992)]

More Articles...