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).

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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

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article

Enantioselective nickel-catalyzed electrochemical reductive conjugate alkenylation of α,β-unsaturated ketones

Syuzanna R. Harutyunyan, Siriphong Somprasong, Bin Wan
3 citations
Chemical Science
Catalytic C–H Functionalization Methods
0.75
article

Enantioselective nickel-catalyzed electrochemical reductive conjugate alkenylation of α,β-unsaturated ketones

Syuzanna R. Harutyunyan, Siriphong Somprasong, Bin Wan
article en
3 citations

Abstract

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).

Chemical ScienceVol. 16(2)
University of Groningen (NL)
China Scholarship Council, European Research Council
Openalex Percentile: Top 31%
Catalytic C–H Functionalization Methods
0.75
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