Hetero[3.1.1]propellanes
[n.1.1]Propellanes are key precursors to bicyclo[n.1.1]alkanes, rigid small-ring hydrocarbons that have emerged as important building blocks in contemporary drug design as bioisosteres for disubstituted benzene rings. [n.1.1]Propellanes featuring heterocyclic rings could enable the direct synthesis of a wide diversity of bridged bicyclic heterocycles, which should exhibit superior physicochemical profiles compared to their established carbocyclic analogues. Here we report the unified synthesis of a family of heterocyclic [3.1.1]propellanes featuring oxygen, nitrogen and sulfur heteroatoms in the three-carbon bridge. The approaches we have developed are necessarily distinct from the established routes to carbocyclic propellanes, and utilize a common precursor that is conveniently assembled on a multigram scale via rhodium-catalysed cyclopropanation. These hetero[3.1.1]propellanes undergo a range of radical ring-opening reactions, affording bridged heterocycles that are of high utility in drug-discovery programmes.
Authors
- Kirsten E. Christensen (ORCID: https://orcid.org/0000-0003-1683-2066)
- Ayan Dasgupta (ORCID: https://orcid.org/0000-0001-9945-8334)
- Edward A. Anderson (ORCID: https://orcid.org/0000-0002-4149-0494)
- Rebecca I. Revie (ORCID: https://orcid.org/0009-0009-2834-8758)
- Yasmine Biddick
- Russell C. Smith
Institutions
- AbbVie (United States) (US)
- University of Oxford (GB)
Publication Details
- Journal
- Nature Chemistry
- Published
- 2026-02-25
- DOI
- https://doi.org/10.1038/s41557-026-02072-2
- Citations
- 1
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 22.95
Funders
- Engineering and Physical Sciences Research Council