| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281922 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
A highly efficient protocol for the Pd-catalyzed regioselective Heck arylation of the electron-rich olefin N-acyl-N-vinylamine with aryl halides has been developed. In the presence of hydrogen-bond donor [H2NiPr2][BF4] as an additive, this proceeds smoothly in isopropanol to afford exclusively the branched products in high yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zhihua Liu, Dan Xu, Weijun Tang, Lijin Xu, Jun Mo, Jianliang Xiao,