Enantioselective nickel-catalyzed electrochemical reductive conjugate alkenylation of α,β-unsaturated ketones
Catalytic electrochemical asymmetric catalysis is emerging as a promising strategy for the synthesis of chiral compounds. Herein, we report an asymmetric electrochemical nickel-catalysed reductive conjugate addition of alkenyl bromides/aryl iodides to α,β-unsaturated ketones in an undivided cell, leading to addition products with high yields and excellent enantioselectivities (up to 96% yield and 96% ee).
Authors
- Syuzanna R. Harutyunyan (ORCID: https://orcid.org/0000-0003-2411-1250)
- Siriphong Somprasong (ORCID: https://orcid.org/0000-0001-6323-5817)
- Bin Wan
Institutions
- University of Groningen (NL)
Publication Details
- Journal
- Chemical Science
- Published
- 2024-11-20
- DOI
- https://doi.org/10.1039/d4sc06891b
- Citations
- 3
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.75
Funders
- China Scholarship Council
- European Research Council