| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5281477 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
Regioselective allylation of enaminones using CuCl2 as the catalyst to give C-allylated products is reported for the first time. The C-allylated products undergo hydrolysis followed by a rearrangement yielding β-keto allyl enamides in excellent yields.
Graphical abstractRegioselective C-allylation of enaminones catalysed by cupric chloride to give β-keto allyl enamides is reported.Download full-size image
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sarangthem Joychandra Singh, Okram Mukherjee Singh,