Abstract
AbstractHybridization of a chiral 3‐hydroxy‐2‐trityl‐pyrrolidine deriving from (R)‐pyrrolidinol with [60]fullerene via click chemistry provides a highly efficient supported enantioselective organocatalyst, which was successfully exploited in a Michael addition of malonates to cinnamaldehydes, via iminium ion activation. The supported organocatalyst was recycled up to six times, with only a moderate decrease in terms of activity and with no loss in enantioselectivity.magnified image
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