Abstract

Highly enantioselective Michael addition of cyclohexanone to aryl nitroolefins in the presence of an ionic liquid anchored pyrrolidine (10 mol%) and TFA (5 mol%) generated the corresponding adducts in high yields (up to 95%) with excellent diastereoselectivities (up to >99:1 dr) and enantioselectivities (up to >99% ee). Furthermore, the catalyst could be recycled and reused at least eight times without loss of its catalytic activity.

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