Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5278225 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
Carbon monoxide-free aminocarbonylation is carried out efficiently via coupling of N,N-dimethylformamide (DMF) with aryl iodides using Pd/C as a heterogeneous catalyst. The catalyst exhibits remarkable activity and is reusable for up to three consecutive cycles. The reaction is applicable to a wide variety of substituted aryl iodides with different steric and electronic properties providing excellent yields of the corresponding tertiary amides.
Graphical abstractCarbon monoxide-free aminocarbonylation reaction is carried out efficiently via coupling of N,N-dimethylformamide (DMF) with aryl iodides using Pd/C as a heterogeneous catalyst.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Pawan J. Tambade, Yogesh P. Patil, Mayur J. Bhanushali, Bhalchandra M. Bhanage,