| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6527721 | Journal of Catalysis | 2013 | 10 Pages |
Abstract
Potassium fluoride has been studied as a non-covalent support for the immobilization through strong hydrogen bond (SHB) of a carboxylic acid containing a chiral pyrrolidine substituent. The resulting system (KF-supCAT) catalyzes the highly diastereo- and enantioselective Michael addition of carbonyl compounds to trans-β-nitrostyrenes, being easily recovered and reused
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Pedro O. Miranda, Carlos Lizandara-Pueyo, Miquel A. Pericà s,