Abstract
Trisubstituted alkenes are important organic synthons and have broad applications in the synthesis of many pharmaceuticals and materials. The stereoselective synthesis of such compounds has long been a research focus for organic researchers. Herein, we report a three-component, reductive cascade, cross-coupling reaction for the arylalkylation of alkynes. A wide range of trisubstituted alkenes are obtained in good to high yields with excellent chemo- and stereoselectivity by switching between electrochemistry and photocatalysis. The E isomer of the product is obtained exclusively when the reaction is conducted with electricity and nickel, while the Z isomer is generated with high stereoselectivity when photo- and nickel dual catalysts are used. Moreover, photo-assisted electrochemically enabled nickel catalyzed protocol is demonstrated to selectively deliver Z-trisubstituted alkenes without the addition of photocatalysts.
Original language | English (US) |
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Journal | Nature Communications |
Volume | 13 |
Issue number | 1 |
DOIs | |
State | Published - Jun 10 2022 |
Bibliographical note
KAUST Repository Item: Exported on 2022-06-13Acknowledged KAUST grant number(s): URF/1/4025
Acknowledgements: This work was financially supported by the King Abdullah University of Science and Technology (KAUST), Saudi Arabia, Office of Sponsored Research (URF/1/4025).
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology
- General Chemistry
- General Physics and Astronomy