CuSO<sub>4</sub>/<i>N</i>-(9<i>H</i>-carbazol-9-yl)picolinamide-Catalyzed C–O Coupling of (Hetero)Aryl Chlorides with Phenols on Water

A Cu-catalyzed C-O coupling of (hetero)aryl chlorides with phenols at 120 °C on water was developed with a designed ligand, <i>N</i>-(9<i>H</i>-carbazol-9-yl)picolinamide (<b>L2</b>). This method features a good substrate scope (both electron-donating and electron-withdrawing), low catalyst/ligand loadings (down to 1 mol %), and excellent scalability and practicability.

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Publication Details

Journal
Organic Letters
Published
2024-08-21
DOI
https://doi.org/10.1021/acs.orglett.4c02620
Citations
7
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.75

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article

CuSO4/N-(9H-carbazol-9-yl)picolinamide-Catalyzed C–O Coupling of (Hetero)Aryl Chlorides with Phenols on Water

Yiqian Wan, Manna Huang, Peng Hong, Fu Chen et al.
7 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.75
article

CuSO4/N-(9H-carbazol-9-yl)picolinamide-Catalyzed C–O Coupling of (Hetero)Aryl Chlorides with Phenols on Water

Yiqian Wan, Manna Huang, Peng Hong, Fu Chen, Xinhai Zhu
article en
7 citations

Abstract

A Cu-catalyzed C-O coupling of (hetero)aryl chlorides with phenols at 120 °C on water was developed with a designed ligand, <i>N</i>-(9<i>H</i>-carbazol-9-yl)picolinamide (<b>L2</b>). This method features a good substrate scope (both electron-donating and electron-withdrawing), low catalyst/ligand loadings (down to 1 mol %), and excellent scalability and practicability.

Organic LettersVol. 26(34)
Sun Yat-sen University (CN)
National Natural Science Foundation of China
Clean water and sanitation
Openalex Percentile: Top 17%
Catalytic C–H Functionalization Methods
1.75
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