Access to pyrrolines and fused diaziridines by selective radical addition to homoallylic diazirines.

ABSTRACT: Pyrroline derivatives are common in bioactive natural products and therapeutic agents. We report here a synthesis of pyrrolines and fused diaziridines by divergent radical cyclization of homoallylic diazirines, which can serve as an internal radical trap and a nitrogen source. This reaction proceeds by selective radical addition to C[double bond, length as m-dash]C or N[double bond, length as m-dash]N bonds followed by intramolecular cyclization. Frontier molecular orbital analysis provides a deep insight into the origin of the selectivity. The reaction demonstrates a new cyclization mode, broad functional group compatibility and high product diversity, and reveals a much broader chemical space for diazirine studies.

SUBMITTER: Ma Z 

PROVIDER: S-EPMC10829008 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature