Asymmetric Ketone Diene Coupling via Stereodivergent Copper Catalysis
We report herein the stereodivergent and enantioselective coupling of ketones with dienes. Under the developed conditions, the reactions of 1,3-butadienyltriisopropylsilane with ketones provide <i>syn</i>-(<i>E</i>)-adducts with excellent enantioselectivities via an α-silyl-(<i>Z</i>)-allylcopper intermediate. By contrast, the reactions between 1,3-dienylboronate and ketones involve an α-boryl-(<i>E</i>)-allylcopper intermediate to give <i>anti</i>-(<i>Z</i>)-adducts with excellent optical purity. The stereodivergence and enantioselectivity of the reactions originate from the distinct allylcopper species involved in the ketone addition step. DFT computational studies provide further evidence to support the analyses.
Authors
- M. Chen
- Diego Paul Chacon Troya
- Zheye Zhang (ORCID: https://orcid.org/0000-0002-2268-5050)
- Jiaming Liu
Institutions
- Institute of Molecular Functional Materials (CN)
- Yangzhou University (CN)
- Virginia Tech (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-02-02
- DOI
- https://doi.org/10.1021/jacs.5c06735
- Citations
- 1
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 22.95