Article ID Journal Published Year Pages File Type
5278225 Tetrahedron Letters 2008 4 Pages PDF
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
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