Base-catalyzed regioselective C(sp3)–Si bond activation of silacyclobutanes and benzosilacyclobutenes
The development of a green, sustainable, and environment-friendly activation model is of great significance in catalytic chemistry. Herein, a transition-metal- and ligand-free, base-catalyzed regioselective C(sp3)–Si bond activation of silacyclobutanes (SCBs) and benzosilacyclobutenes (BSBs) has been developed. The protocol features a simple catalytic system that proceeds smoothly under air atmosphere without requiring inert gas protection. A variety of SCBs and BSBs are competent substrates, along with a range of nucleophiles as coupling partners. Furthermore, the strategy provides a straightforward platform for the late-stage functionalization of various bioactive molecules, enabling access to diverse quaternary silicon-containing scaffolds. Preliminary mechanistic investigations indicate that the C–Si bond cleavage is involved in the rate-determining step, and the hydrogen source originates from the nucleophile. In addition, the proposed mechanism is consistent with our experimental results and further supported by DFT calculations. Herein, a transition-metal- and ligand-free, base-catalyzed regioselective C(sp3)–Si bond activation of silacyclobutanes (SCBs) and benzosilacyclobutenes (BSBs) has been developed.
Authors
- Delong Mu (ORCID: https://orcid.org/0000-0003-2914-7949)
- Yuanfang Kong
Institutions
- Southern University of Science and Technology (CN)
- Henan Institute of Technology (CN)
- First Affiliated Hospital of Henan University (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-07-16
- DOI
- https://doi.org/10.1038/s41467-026-75467-x
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00