Tunable [3+2] and [4+2] annulations for pyrrolidine and piperidine synthesis

Chem Commun (Camb). 2023 May 23;59(42):6418-6421. doi: 10.1039/d3cc01400b.

Abstract

N-heterocycles are privileged pharmaceutical scaffolds in drug discovery and development. We disclose here divergent intermolecular coupling strategies that can access diverse N-heterocycles directly from olefins. The radical-to-polar mechanistic switching is key for the divergent cyclization processes. These distinctive annulations result in the coupling of alkenes with simple bifunctional reagents for divergent N-heterocycle syntheses.