Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5277260 | Tetrahedron Letters | 2011 | 6 Pages |
A novel approach was adopted for the synthesis of a series of chromonyl chalcones (3a-o) from 3-formylchromones (1a-c) and different cyclic active methyl compounds (2a-e), employing Zn(l-proline)2 as a recyclable Lewis acid catalyst in water. In each conversion, the catalyst was successfully recovered and reused several times without significant loss in yield and selectivity. All the newly synthesized compounds were characterized using elemental analysis and spectral data (IR, 1H NMR, 13C NMR and mass spectrometry).
Graphical abstractA novel synthesis of a series of chromonyl chalcones (3a-o) was achieved by the reaction of 3-formylchromones (1a-c) and active methyl compounds (2a-e) in excellent yields, using recyclable Zn(l-proline)2 Lewis acid catalyst in green solvent water.Download full-size image