Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5225375 | Tetrahedron | 2007 | 5 Pages |
Abstract
The cyclopalladated ferrocenylimine was an efficient catalyst for the borylation/Suzuki coupling reaction. The catalytic loading for the reaction containing bromoarenes was 1 mol %. When iodobenzene was used, the catalytic loading was as low as 0.1 mol %. Furthermore, the cyclopalladated ferrocenylimine also exhibited excellent catalytic power in the case of substrates containing electron-donating substituents, with yields reaching 93% or higher.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ning Ma, Zhiwu Zhu, Yangjie Wu,