In divergent carbonylative transformations using identical starting substrates, ligand-assisted transition metal catalysis has dominated selectively controllable transformations, but achieving precise control of CO insertion in transition-metal-free systems remains a challenge. Here, the authors disclose a divergent radical tandem carbonylation of multisubstituted homoallylic alcohols for the synthesis of γ-lactones and 1,4-diones.
- Yuanrui Wang
- Youzhi Xu
- Xiao-Feng Wu