Electrochemical Annulation of <i>p</i>-Alkoxy or <i>p</i>-Hydroxy Anilines with Enaminones for Selective Indole and Benzofuran Synthesis

The green and sustainable electrochemical oxidative cyclization of enaminones with <i>p</i>-methoxy/<i>p</i>-hydroxy anilines has been developed, enabling the regioselective synthesis of indoles and benzofurans. The methods are of significant advantage not only due to the mild and metal-free sustainable electrochemical conditions, but also because of the employment of easily available and stable aniline substrates to replace the unstable quinoneimide for a similar annulation in previous work.

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Publication Details

Journal
Organic Letters
Published
2025-03-11
DOI
https://doi.org/10.1021/acs.orglett.4c04572
Citations
20
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
18.72

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article

Electrochemical Annulation of p-Alkoxy or p-Hydroxy Anilines with Enaminones for Selective Indole and Benzofuran Synthesis

Lihua Liao, Zukang Zhong, Jie‐Ping Wan, Yunyun Liu
20 citations
Organic Letters
Radical Photochemical Reactions
18.72
article

Electrochemical Annulation of p-Alkoxy or p-Hydroxy Anilines with Enaminones for Selective Indole and Benzofuran Synthesis

Lihua Liao, Zukang Zhong, Jie‐Ping Wan, Yunyun Liu
article en
20 citations

Abstract

The green and sustainable electrochemical oxidative cyclization of enaminones with <i>p</i>-methoxy/<i>p</i>-hydroxy anilines has been developed, enabling the regioselective synthesis of indoles and benzofurans. The methods are of significant advantage not only due to the mild and metal-free sustainable electrochemical conditions, but also because of the employment of easily available and stable aniline substrates to replace the unstable quinoneimide for a similar annulation in previous work.

Organic LettersVol. 27(11)
Shaoyang University (CN), Jiangxi Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province
Openalex Percentile: Top 0%
Radical Photochemical Reactions
18.72
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