Asymmetric Conjugate Addition of Ketones to Maleimides Organocatalyzed by a Chiral Primary Amine-Salicylamide

Enantioenriched substituted succinimides are interesting compounds, and their asymmetric organocatalytic synthesis by the conjugated addition of ketones to maleimides has been scarcely explored. This study shows the enantioselective conjugate addition of ketones to maleimides organocatalyzed by a simple primary amine-salicylamide derived from a chiral trans-cyclohexane-1,2-diamine, which provides the desired succinimides in good to excellent yields (up to 98%) and with moderate to excellent enantioselectivities (up to 99%).

Automated summary

This study demonstrates the enantioselective synthesis of succinimides by the conjugated addition of ketones to maleimides, catalyzed by a simple primary amine-salicylamide. The reaction gives the desired compounds in good to excellent yields and with moderate to excellent enantioselectivities.