Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000131.xml
Synfacts 2009(8): 0891-0891
DOI: 10.1055/s-0029-1217420
DOI: 10.1055/s-0029-1217420
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Epoxidation of α,β-Unsaturated Ketones with a Self-Supported BINOL-Zn Complex
H. Wang, Z. Wang, K. Ding*
Shanghai Institute of Organic Chemistry, P. R. of China
Further Information
Publication History
Publication Date:
23 July 2009 (online)
Significance
Previously M. Bougauchi and co-workers have developed self-supported BINOL-La-Ph3PO catalysts (J. Am. Chem. Soc. 1997, 119, 2329) for asymmetric epoxidation of α,β-unsaturated ketones. In search of more efficient systems for this reaction, the authors have found Zn complexes using BINOL dimer. L1 produces an isolable white solid which is virtually insoluble in common organic solvents. This complex could catalyze the title reaction to provide epoxides in high yield and ee values. Further, the catalyst can be reused without significant loss of activity.