[n.1.1]Propellanes are versatile precursors to bicyclo[n.1.1]alkane benzene bioisosteres, but heterocyclic variants have eluded synthesis. Now, a unified synthetic strategy has been developed to access hetero[3.1.1]propellanes on multigram scale. Their ring-opening under radical conditions affords a variety of heterobicyclo[3.1.1]heptanes, which are important motifs in drug design.
- Rebecca I. Revie
- Ayan Dasgupta
- Edward A. Anderson