Low-Valent Tungsten Catalyzed Carbonylative Synthesis of Benzoates from Aryl Iodides and Alcohols

Non-noble metals catalyzed carbonylative reactions serve as straightforward and sustainable methods for the synthesis of functionalized carbonyl-containing compounds. Herein, a low-valent-tungsten-catalyzed reaction that enables the coupling of aryl iodides and alcohols or phenols was disclosed, employing the readily available W(CO)<sub>6</sub> as the effective catalyst and PPh<sub>3</sub> as ligand. Under the optimal reaction conditions, aryl iodides smoothly underwent carbonylative coupling reactions with alcohols or phenols, processing the feature of broad substrate scope and good functional groups tolerance. Furthermore, this conversion can be carried out on a gram scale, showcasing significant promise in the synthesis of pharmaceutical or biologically active compounds.

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Publication Details

Journal
Molecules
Published
2024-11-10
DOI
https://doi.org/10.3390/molecules29225305
Citations
1
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.25

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article

Low-Valent Tungsten Catalyzed Carbonylative Synthesis of Benzoates from Aryl Iodides and Alcohols

Zhaoyang Huang, Feihua Ye, Lu Lin, Chunsheng Li et al.
1 citations
Molecules
Catalytic Cross-Coupling Reactions
0.25
article

Low-Valent Tungsten Catalyzed Carbonylative Synthesis of Benzoates from Aryl Iodides and Alcohols

Zhaoyang Huang, Feihua Ye, Lu Lin, Chunsheng Li, Xiang Li, Lixuan Huang, Yunwei Huang
article en
1 citations

Abstract

Non-noble metals catalyzed carbonylative reactions serve as straightforward and sustainable methods for the synthesis of functionalized carbonyl-containing compounds. Herein, a low-valent-tungsten-catalyzed reaction that enables the coupling of aryl iodides and alcohols or phenols was disclosed, employing the readily available W(CO)<sub>6</sub> as the effective catalyst and PPh<sub>3</sub> as ligand. Under the optimal reaction conditions, aryl iodides smoothly underwent carbonylative coupling reactions with alcohols or phenols, processing the feature of broad substrate scope and good functional groups tolerance. Furthermore, this conversion can be carried out on a gram scale, showcasing significant promise in the synthesis of pharmaceutical or biologically active compounds.

MoleculesVol. 29(22)
Zhaoqing University (CN)
Basic and Applied Basic Research Foundation of Guangdong Province
Responsible consumption and production
Openalex Percentile: Top 47%
Catalytic Cross-Coupling Reactions
0.25
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