Journal of the American Chemical Society 2012-10-24

Palladium-catalyzed regioselective carbonylation of C-H bonds of N-alkyl anilines for synthesis of isatoic anhydrides.

Zheng-Hui Guan, Ming Chen, Zhi-Hui Ren

Index: J. Am. Chem. Soc. 134(42) , 17490-3, (2012)

Full Text: HTML

Abstract

A Pd-catalyzed regioselective C-H bond carbonylation of N-alkyl anilines for the synthesis of isatoic anhydrides has been developed. The key Pd-catalyst intermediate has been isolated and characterized. This novel Pd-catalyzed carbonylation reaction tolerates a wide range of functional groups and is a reliable method for the rapid elaboration of readily available N-alkyl anilines into a variety of substituted isatoic anhydrides under mild conditions.


Related Compounds

Related Articles:

Hydrogen-bonding in 2-aminobenzoyl-alpha-chymotrypsin formed by acylation of the enzyme with isatoic anhydride: IR and mass spectroscopic studies.

2002-01-04

[ChemBioChem. 3(1) , 68-75, (2002)]

Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids.

2011-11-18

[Org. Lett. 13 , 6114-6117, (2011)]

1,3-Dipolar cycloaddition-decarboxylation reactions of an azomethine ylide with isatoic anhydrides: formation of novel benzodiazepinones.

2011-02-04

[Org. Lett. 13(3) , 486-9, (2011)]

Suicide enzyme inactivators.

1983-01-01

[Basic Life Sci. 25 , 287-305, (1983)]

Synthesis of 2,3-dihydroquinazolin-4(1H)-ones by three-component coupling of isatoic anhydride, amines, and aldehydes catalyzed by magnetic Fe(3)O(4) nanoparticles in water.

2010-09-13

[J. Comb. Chem. 12(5) , 643-6, (2010)]

More Articles...