Catalytic Ring Expansion of Furyl Hydrosilanes: Synthesis of 1,2‐Oxasilines as Diels‐Alder Diene Components
The development of new methods for aromatic ring-expansion offers a strategic means of transforming abundant aromatic feedstocks into intricate structures via skeletal editing, thereby unlocking valuable avenues for organic synthesis. We report herein a mild and efficient ruthenium-catalyzed ring-expansion of 2-silylfurans to form 1,2-oxasilines with wide substrate scope and excellent functional group tolerance. Density functional theory (DFT) calculations suggest the reaction proceeds through regioselective insertion of furan double bond into a Ru─H bond, followed by skeletal rearrangement, 1,2-hydride transfer, and elimination steps. The resulting 1,2-oxasilines are electron-rich cyclic dienes with an extrudable and transformable Si─O linker, which exhibit unique and versatile reactivity in Diels-Alder cyclization with electron-deficient dienophiles, enabling modular assembly of molecular skeletons with higher complexity.
Authors
- Xin Hong (ORCID: https://orcid.org/0000-0003-4717-2814)
- Qiaoxing He
- Zheng Huang (ORCID: https://orcid.org/0000-0001-7524-098X)
- Yao Fu (ORCID: https://orcid.org/0000-0003-4103-0065)
- Huaquan Fang (ORCID: https://orcid.org/0000-0003-2763-1497)
- Sifan Liu (ORCID: https://orcid.org/0000-0002-1608-4216)
- Xi Lu (ORCID: https://orcid.org/0000-0002-9338-0780)
- Guixia Liu (ORCID: https://orcid.org/0000-0001-7565-2183)
- Zheyuan Xu
Institutions
- University of Science and Technology (YE)
- University of Science and Technology of China (CN)
- Chongqing University (CN)
- Chinese Academy of Sciences (CN)
- ShanghaiTech University (CN)
- Shanghai Institute of Organic Chemistry (CN)
- Material Sciences (United States) (US)
- State Key Laboratory of Organometallic Chemistry
- Zhejiang University (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2025-03-22
- DOI
- https://doi.org/10.1002/anie.202425232
- Citations
- 1
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.94