ElectrochemicalAnnulation of <i>p</i>‑Alkoxyor <i>p</i>‑Hydroxy Anilines with Enaminones forSelective 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.

Publication Details

Journal
Figshare
Published
2025-03-11
DOI
https://doi.org/10.1021/acs.orglett.4c04572.s001
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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ElectrochemicalAnnulation of p‑Alkoxyor p‑Hydroxy Anilines with Enaminones forSelective Indole and Benzofuran Synthesis

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Catalytic C–H Functionalization Methods
article

ElectrochemicalAnnulation of p‑Alkoxyor p‑Hydroxy Anilines with Enaminones forSelective Indole and Benzofuran Synthesis

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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.

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Openalex Percentile: Top 63%
Catalytic C–H Functionalization Methods
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