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.

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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
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article

Asymmetric Ketone Diene Coupling via Stereodivergent Copper Catalysis

M. Chen, Diego Paul Chacon Troya, Zheye Zhang, Jiaming Liu
1 citations
Journal of the American Chemical Society
Organoboron and organosilicon chemistry
22.95
article

Asymmetric Ketone Diene Coupling via Stereodivergent Copper Catalysis

M. Chen, Diego Paul Chacon Troya, Zheye Zhang, Jiaming Liu
article en
1 citations

Abstract

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.

Journal of the American Chemical SocietyVol. 148(5)
Institute of Molecular Functional Materials (CN), Yangzhou University (CN), Virginia Tech (US)
Openalex Percentile: Top 1%
Organoboron and organosilicon chemistry
22.95
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