摘要
A simple and efficient process for an exclusive mono-Michael addition of active methylene compounds to conjugated esters, nitriles and ketones is developed. An ionic liquid-mediated reaction is carried out at room temperature. A reaction carried out at 60 degrees C resulted in a double-addition product. A mechanism is proposed and supported by P-31 and DOSY NMR analysis of the used ionic liquid.
- 出版日期2015