Highly Enantioselective Synthesis of Optically Active Ketones by Iridium-Catalyzed Asymmetric Hydrogenation
Close to perfect enantioselectivity (up to 99 % ee, see scheme) is found for the formation of α‐substituted ketones by the asymmetric hydrogenation of enones with an iridium–phosphinooxazoline catalyst. In an operationally simple process, both linear and cyclic substrates react well and afford the d...
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Veröffentlicht in: | Angewandte Chemie (International ed.) 2008-01, Vol.47 (46), p.8920-8923 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Close to perfect enantioselectivity (up to 99 % ee, see scheme) is found for the formation of α‐substituted ketones by the asymmetric hydrogenation of enones with an iridium–phosphinooxazoline catalyst. In an operationally simple process, both linear and cyclic substrates react well and afford the desired products in high yields. A wide variety of substituents are tolerated, thus making the method synthetically appealing. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.200803709 |