| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1350277 | Tetrahedron: Asymmetry | 2008 | 5 Pages |
Abstract
Chiral Schiff-bases 2, 3, 4 and 5 were designed for the enantioselective nitroaldol (Henry) reaction. The highest enantioselectivity was observed for ligand 4 (82% ee) when CH2Cl2 was used as a solvent.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Mehmet Ãolak, Nadir Demirel,