| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7767179 | Tetrahedron: Asymmetry | 2014 | 6 Pages |
Abstract
An effective protocol for the stereoselective Michael addition of aldehydes to nitroolefins using pyrrolidine-pyrazole as an organocatalyst is described. The catalytic cycle was found to be productive in terms of yield and selectivity, when performed under solvent-free reaction conditions and employing 15 mol % of catalyst and 10 mol % of benzoic acid at room temperature.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Togapur Pavan Kumar,