摘要

A chiral anion modified ionic liquid derived from L-proline proves as a green and efficient asymmetric organocatalyst for direct asymmetric aldol reactions in [BMIm]BF4 at room temperature. The corresponding aldol products with moderate to good isolated yields (up to 99%), anti-diastereoselectivities (up to 97:3), and excellent enantioselectivities (up to 99% ee) were afforded. Recycling of the catalyst and solvent ([BMIm]BF4) was possible up to four runs with a slight reduction in activity.