Epoxide Synthesis via Energy-Transfer-Enabled 1,4-Nitrogen Migration
Abstract Epoxides are privileged scaffolds in synthetic chemistry, serving as key precursors for amino alcohols and pharmaceuticals. Traditional strategies to access valuable α-amino epoxides often face limitations in selectivity and require harsh conditions. Inspired by the classic di-π-methane rearrangement, we have developed a visible-light-driven alternative that triggers an unprecedented 1,4-nitrogen migration via an oxa-π,σ-methane rearrangement mechanism. This energy-transfer-catalysis process efficiently converts readily available allylic alcohols into α-amino-substituted epoxides under mild conditions. This method provides a direct and versatile route to these high-value building blocks, bypassing previous synthetic bottlenecks. We describe the discovery and mechanical insights of this new reaction paradigm in detail.
Authors
- Qiu-Zhu Wang
- Huan‐Ming Huang (ORCID: https://orcid.org/0000-0001-9461-6508)
- Jian‐Quan Weng (ORCID: https://orcid.org/0000-0001-5513-6421)
- Wen-Tao Wu
Institutions
- Nankai University (CN)
- ShanghaiTech University (CN)
- Shanghai Advanced Research Institute (CN)
- Shanghai Institute of Organic Chemistry (CN)
- Zhejiang University of Technology (CN)
Publication Details
- Journal
- Synlett
- Published
- 2025-11-24
- DOI
- https://doi.org/10.1055/a-2735-9496
- Citations
- 1
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.94