| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1347499 | Tetrahedron: Asymmetry | 2013 | 5 Pages |
Abstract
An efficient protocol for the enantioselective Michael additions of ketones to chalcones catalyzed by a hydroxyphthalimide linked triazole–pyrrolidine derivative has been developed. The corresponding products, 1,5-dicarbonyl compounds, were obtained in good yields with high levels of stereoselectivities under mild reaction conditions employing benzoic acid as an additive.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Togapur Pavan Kumar, Mohammad Abdul Sattar, Vanka Uma Maheshwara Sarma,