Palladium-Catalyzed Dual C–H Arylation/Cyclization Reaction of Iodoferrocenes with <i>ortho</i>-Bromobenzamides for the Construction of Arylated Isoquinolone-Fused Ferrocenes

We reported a palladium/norbornene-catalyzed dual intermolecular C-H arylation/intramolecular cyclization reaction of iodoferrocenes with <i>ortho</i>-bromobenzamides, enabling the formation of arylated isoquinolone-fused ferrocenes in a straightforward and effective manner. This method has a broad substrate scope and good functional group compatibility, while the gram-scale reaction demonstrates the practicality of this method.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-12-12
DOI
https://doi.org/10.1021/acs.joc.4c02128
Citations
4
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.00

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article

Palladium-Catalyzed Dual C–H Arylation/Cyclization Reaction of Iodoferrocenes with ortho-Bromobenzamides for the Construction of Arylated Isoquinolone-Fused Ferrocenes

Jingwen Fan, Guolin Cheng, Zhiyong Li, Yuhao Ding et al.
4 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
1.00
article

Palladium-Catalyzed Dual C–H Arylation/Cyclization Reaction of Iodoferrocenes with ortho-Bromobenzamides for the Construction of Arylated Isoquinolone-Fused Ferrocenes

Jingwen Fan, Guolin Cheng, Zhiyong Li, Yuhao Ding, Hailin Guo, Jingyu Li
article en
4 citations

Abstract

We reported a palladium/norbornene-catalyzed dual intermolecular C-H arylation/intramolecular cyclization reaction of iodoferrocenes with <i>ortho</i>-bromobenzamides, enabling the formation of arylated isoquinolone-fused ferrocenes in a straightforward and effective manner. This method has a broad substrate scope and good functional group compatibility, while the gram-scale reaction demonstrates the practicality of this method.

The Journal of Organic ChemistryVol. 89(24)
Huaqiao University (CN), Jiangxi Normal University (CN)
National Natural Science Foundation of China, Xiamen University
Openalex Percentile: Top 26%
Catalytic C–H Functionalization Methods
1.00
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