| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275943 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
A highly efficient asymmetric Michael addition of anthrone to nitroalkenes catalyzed by cinchona alkaloids was described. Up to 99% ee of the corresponding adduct was obtained.
Graphical abstractA highly efficient asymmetric Michael addition of anthrone to nitroalkenes catalyzed by cinchona alkaloids was described. Up to 99% ee of the corresponding adduct was obtained.Figure optionsDownload full-size imageDownload as PowerPoint slide
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