Electrochemically Induced Regio‐ and Stereoselective ( E )‐β‐C(sp 2 )─H Alkoxycarbonylation of Enamides With Carbazates

Herein, we disclosed an electrochemically induced alkoxycarbonylation of enamides with carbazates under metal‐free and peroxide‐free reaction conditions, which provided a green protocol for constructing enol esters, exhibiting excellent regioselectivity and mainly affording products in the E ‐configuration. Mechanistically, a free alkoxycarbonyl radical pathway was involved in this approach.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-09-29
DOI
https://doi.org/10.1002/adsc.70785
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Electrochemically Induced Regio‐ and Stereoselective ( E )‐β‐C(sp 2 )─H Alkoxycarbonylation of Enamides With Carbazates

Ling Yang, Haiqing Luo, Xiaolan Li, Yiyan Lin et al.
Advanced Synthesis & Catalysis
Radical Photochemical Reactions
article

Electrochemically Induced Regio‐ and Stereoselective ( E )‐β‐C(sp 2 )─H Alkoxycarbonylation of Enamides With Carbazates

Ling Yang, Haiqing Luo, Xiaolan Li, Yiyan Lin, Guisheng Chen, Xuzhong Luo, Yucheng Yang
article en

Abstract

Herein, we disclosed an electrochemically induced alkoxycarbonylation of enamides with carbazates under metal‐free and peroxide‐free reaction conditions, which provided a green protocol for constructing enol esters, exhibiting excellent regioselectivity and mainly affording products in the E ‐configuration. Mechanistically, a free alkoxycarbonyl radical pathway was involved in this approach.

Advanced Synthesis & CatalysisVol. 368(20)
Gannan Normal University (CN)
Openalex Percentile: Top 23%
Radical Photochemical Reactions
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