Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5269733 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
The cross-coupling reaction between aryl halides with aqueous ammonia was efficiently catalyzed in CuI/PEG-400 System with high yield. A range of electron-withdrawing or electron-donating aryl iodides and bromides were found to be applicable to the environmentally benign system. The process allows assembly of primary arylamines in great diversity which bear a wide range of functional groups including cyano, nitro, acetyl, ether, or amino moiety.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Junmin Chen, Tangjun Yuan, Wenyan Hao, Mingzhong Cai,