This work was financially supported by the National Natural Science Foundation of China (No. 20272037) and the Doctor's Foundation of Education Ministry of China (No. 20030610022). The authors thank Prof. Xian-Deng Hou for his kind help during the preparation of the manuscript.
Communication
Heterogeneous Enantioselective Hydrogenation of Aromatic Ketones Catalyzed by Cinchona- and Phosphine-Modified Iridium Catalysts†
Article first published online: 8 AUG 2008
DOI: 10.1002/anie.200801809
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Angewandte Chemie International Edition
Volume 47, Issue 48, pages 9240–9244, November 17, 2008
Additional Information
How to Cite
Jiang, H.-y., Yang, C.-f., Li, C., Fu, H.-y., Chen, H., Li, R.-x. and Li, X.-j. (2008), Heterogeneous Enantioselective Hydrogenation of Aromatic Ketones Catalyzed by Cinchona- and Phosphine-Modified Iridium Catalysts. Angew. Chem. Int. Ed., 47: 9240–9244. doi: 10.1002/anie.200801809
- †
Publication History
- Issue published online: 12 NOV 2008
- Article first published online: 8 AUG 2008
- Manuscript Revised: 7 JUL 2008
- Manuscript Received: 17 APR 2008
Funded by
- National Natural Science Foundation of China. Grant Number: 20272037
- Doctor's Foundation of Education Ministry of China. Grant Number: 20030610022
Keywords:
- alkaloids;
- asymmetric catalysis;
- iridium;
- ketones;
- supported catalysts

Catalyst support: The first highly enantioselective heterogeneous hydrogenation of aromatic ketones catalyzed by Ir/SiO2 stabilized with Ph3P and modified by a chiral diamine derived from a cinchona alkaloid is described (see scheme). The reaction can be employed for the reduction of a broad range of aromatic ketones to the corresponding alcohols with high enantioselectivity.

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