ArticleRSC advances2025
Electrochemical dearomatization of 2-naphthols for C-O bond formation.
Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
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No grant is acknowledged in the PubMed record.
Abstract
We reported a metal-free electrochemical oxidative C-O homocoupling of 2-naphthols, followed by subsequent alkoxylation under mild conditions. This strategy offered an eco-friendly and cost-effective electrochemical approach using undivided cells. Additionally, the reaction exhibited broad tolerance to various substituted 2-naphthols and diverse alcohols, affording the corresponding naphthalenones in moderate to good yields.
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Registered trials
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