Selective hydrogenation of exocyclic α,β-unsaturated ketones:: Part I. Hydrogenations over palladium
✍ Scribed by Gabriella Fogassy; László Hegedűs; Antal Tungler; Albert Lévai; Tibor Máthé
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 261 KB
- Volume
- 154
- Category
- Article
- ISSN
- 1381-1169
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✦ Synopsis
Exocyclic a ,b-unsaturated ketones were hydrogenated to the corresponding saturated ketones with Pd catalysts. The effect of solvents, basic and poisoning additives and various supports on conversion and selectivity was investigated. The conditions, under which the reaction afforded the saturated ketones with complete selectivity and appropriate reaction rate, were determined. The highest selectivities were obtained over PdrC, in toluene, at atmospheric pressure and in the presence of pyridine.
📜 SIMILAR VOLUMES
In the asymmetric synthesis of chiral compounds, the reduction of prochiral unsaturated reactants has a great importance. (S)-proline as a chiral auxiliary is used in the hydrogenations of exocyclic ␣,-unsaturated ketones with palladium on carbon catalysts, producing the corresponding saturated ke