Aminoquinoline-Directed Electrochemical Cobalt-Catalyzed C(sp²)–H Alkoxylation

Electrochemically, earth-abundant cobalt(II)-catalyzed C(sp<sup>2</sup>)-H alkoxylation of ferrocenyl and arenyl amides with 8-aminoquinoline directing groups was developed under mild, oxidant-free conditions. This protocol afforded a broad range of alkoxylated products in moderate to high yields, employing readily available alcohols as both alkoxy sources and green solvents. Notably, this method enabled efficient C-O bond formation via sustainable electrolysis and offered a practical route to alkylated organic compounds.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-10-02
DOI
https://doi.org/10.1021/acs.joc.5c01585
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Aminoquinoline-Directed Electrochemical Cobalt-Catalyzed C(sp²)–H Alkoxylation

Mengli Yang, Xing‐Wang Wang, Bojun Zhang, Zhi‐Xiong Ou et al.
1 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.94
article

Aminoquinoline-Directed Electrochemical Cobalt-Catalyzed C(sp²)–H Alkoxylation

Mengli Yang, Xing‐Wang Wang, Bojun Zhang, Zhi‐Xiong Ou, Jun‐Qi Zhang, Libo Li
article en
1 citations

Abstract

Electrochemically, earth-abundant cobalt(II)-catalyzed C(sp<sup>2</sup>)-H alkoxylation of ferrocenyl and arenyl amides with 8-aminoquinoline directing groups was developed under mild, oxidant-free conditions. This protocol afforded a broad range of alkoxylated products in moderate to high yields, employing readily available alcohols as both alkoxy sources and green solvents. Notably, this method enabled efficient C-O bond formation via sustainable electrolysis and offered a practical route to alkylated organic compounds.

The Journal of Organic ChemistryVol. 90(40)
Soochow University (CN), Laboratoire de Synthèse Organique (FR), Taizhou University (CN)
Openalex Percentile: Top 21%
Catalytic C–H Functionalization Methods
0.94
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