Synfacts 2006(1): 0035-0035  
DOI: 10.1055/s-2005-921737
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Heterogeneous Catalyst for Enantioselective Epoxidation of α,β-Unsaturated Ketones

Contributor(s): Hisashi Yamamoto, Matthew B. Boxer
X. Wang, L. Shi, M. Li, K. Ding*
Shanghai Institute of Organic Chemistry and Shanhai University, P. R. of China
Further Information

Publication History

Publication Date:
16 December 2005 (online)

Significance

Highly enantioselective epoxidation of α,β-unsaturated ketones with cumene hydro­peroxide is accomplished with heterogenization of Shibasaki’s Binol/La catalyst. While many different linkers were tested with different topologies the simple 1,4-ethynyl-phenylene showed consistently high yields and enantioselectivities. The catalyst was formed by addition of the chiral unit to a solution of the metal in THF. The precipitated solid catalyst was shown to have high activity and selectivity through six runs at a loading of 5 mol%.