Electrochemical reduction of unsaturated carbon–carbon bonds via 3d transition-metal catalysis

Electrochemical reduction has emerged as a powerful alternative to conventional hydrogenation for unsaturated C–C bonds, enabling precise control without molecular hydrogen or stoichiometric reductants. This review summarizes recent advances in iron-, cobalt-, and nickel-catalyzed electroreduction of alkynes and alkenes, highlighting how electrochemical parameters and catalyst design unlock distinct, controllable reaction manifolds that are inaccessible under thermochemical conditions. These developments position 3d metal electrocatalysis as a versatile and programmable platform for selective hydrogenation and isotopic labeling under mild, sustainable conditions.

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Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2026-06-17
DOI
https://doi.org/10.3762/bjoc.22.75
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Electrochemical reduction of unsaturated carbon–carbon bonds via 3d transition-metal catalysis

Cheoljae Kim, Isaac Choi, Minki Jeon, Geon Kang et al.
Beilstein Journal of Organic Chemistry
Radical Photochemical Reactions
article

Electrochemical reduction of unsaturated carbon–carbon bonds via 3d transition-metal catalysis

Cheoljae Kim, Isaac Choi, Minki Jeon, Geon Kang, Pooja Kumari Jat
article en

Abstract

Electrochemical reduction has emerged as a powerful alternative to conventional hydrogenation for unsaturated C–C bonds, enabling precise control without molecular hydrogen or stoichiometric reductants. This review summarizes recent advances in iron-, cobalt-, and nickel-catalyzed electroreduction of alkynes and alkenes, highlighting how electrochemical parameters and catalyst design unlock distinct, controllable reaction manifolds that are inaccessible under thermochemical conditions. These developments position 3d metal electrocatalysis as a versatile and programmable platform for selective hydrogenation and isotopic labeling under mild, sustainable conditions.

Beilstein Journal of Organic ChemistryVol. 22
Chungbuk National University (KR)
Ministry of Education, National Research Foundation, Chungbuk National University, National Research Foundation of Korea, Ministry of Education, India, Ministry of Science and ICT, South Korea
Responsible consumption and production
Openalex Percentile: Top 13%
Radical Photochemical Reactions
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