科研之友
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摘要
We disclose herein an efficient enantioselective organocatalytic Michael reaction between alpha, beta-unsaturated ketones and malonic acid half thioesters (MAHTs). The reactions are catalyzed by a primary amine to generate Michael addition products in good to excellent yields (62-87%) with high to excellent enantioselectivities (80-98%).
- 出版日期2015
- 单位湖北科技学院
