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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.


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Enantioselective hydrogenation of exocyc
✍ Gabriella Fogassy; Antal Tungler; Albert Lévai; Gábor Tóth 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 74 KB

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