Propellane-free access to bicyclo[1.1.1]pentanes
Bicyclo[1.1.1]pentane (BCP) has emerged over the past decade as a valuable three-dimensional bioisostere for benzene, attracting considerable interest in pharmaceutical research for its ability to improve drug-like properties. Although [1.1.1]propellane has traditionally served as the key precursor to mono- and 1,3- disubstituted BCPs, the growing demand for multisubstituted and bridge-functionalized BCP derivatives has spurred the development of alternative, propellane-free synthetic strategies. Recent advances toward these highly strained and sterically hindered ring systems can be broadly organized into three mechanistic categories: intramolecular diradical couplings, carbene-mediated ring expansions, and two-electron disconnections. This Perspective highlights these emerging methodologies, assesses their scope and limitations, and offers an outlook on remaining synthetic challenges and their implications for medicinal chemistry.
Authors
- Yuzuru Kanda (ORCID: https://orcid.org/0000-0003-2200-2667)
- Rohan R. Merchant (ORCID: https://orcid.org/0000-0002-5472-8780)
- Chang Liu
- Renzhe Li
- Tian Qin
- Wenyuan Li
Institutions
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- Southwestern Medical Center (US)
- Novartis (United States) (US)
- The University of Texas Southwestern Medical Center (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-01-12
- DOI
- https://doi.org/10.1038/s41467-026-68309-3
- Primary Topic
- Cyclopropane Reaction Mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation
- National Institutes of Health
- Division of Chemistry