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

A Cu-catalyzed\nC–O coupling of (hetero)­aryl chlorides with\nphenols 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\nand electron-withdrawing), low catalyst/ligand loadings (down to 1\nmol %), and excellent scalability and practicability.

Publication Details

Journal
Figshare
Published
2024-08-21
DOI
https://doi.org/10.1021/acs.orglett.4c02620.s001
Primary Topic
Diverse Scientific and Economic Studies
Type
article
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article

CuSO4/N‑(9H‑carbazol-9-yl)picolinamide-Catalyzed\nC–O\nCoupling of (Hetero)Aryl Chlorides with Phenols on Water

Figshare
Diverse Scientific and Economic Studies
article

CuSO4/N‑(9H‑carbazol-9-yl)picolinamide-Catalyzed\nC–O\nCoupling of (Hetero)Aryl Chlorides with Phenols on Water

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Abstract

A Cu-catalyzed\nC–O coupling of (hetero)­aryl chlorides with\nphenols 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\nand electron-withdrawing), low catalyst/ligand loadings (down to 1\nmol %), and excellent scalability and practicability.

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Openalex Percentile: Top 49%
Diverse Scientific and Economic Studies
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CuSO<sub>4</sub>/<i>N</i>‑(9<i>H</i>‑carbazol-9-yl)picolinamide-Catalyzed\nC–O\nCoupling of (Hetero)Aryl Chlorides with Phenols on Water · Figshare (2024) | TGRS Research Map | TGRS