| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5292121 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A simple Ni-catalysed cross-coupling protocol for amino-heteroaryl chlorides with alkylzinc reagents has been developed. The alkylzinc reagents can be commercially available dialkylzincs or alkylzinc halides, or can be conveniently generated in situ from diethylzinc and primary alkyl bromides in the presence of the same inexpensive Ni catalyst used to effect the subsequent coupling reaction.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Iain A.S. Walters,