Visible light-mediated cyclopropylamides [3+2] cycloaddition with maleimides to synthesize cyclopentylamide derivatives
Abstract
The [3+2] cyclization is one of the most common reactions for constructing five-membered rings. In this study, we present a detailed synthetic methodology of [3 + 2] cyclization of N-acyl cyclopropylamines and N-substituted maleimides photocatalyzed by 10-methyl-9-homotrimelylacridine perchlorate. A series of stable N-acyl cyclopentylamine derivatives was prepared under mild conditions.
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