| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1322918 | Journal of Organometallic Chemistry | 2016 | 4 Pages |
Abstract
•The oxidative coupling reaction of anilides with olefins.•N-aryl rings products were achieved under non-acidic conditions.•Catalytic activity is improved by non-coordinating anions.
CH bond activation is an important issue. The Pd-catalyzed and non-coordinating anion improved CH bond activation was realized through the oxidative coupling reaction of anilides with olefins under non-acidic conditions. Additionally, the catalytic activity of palladium catalysts is enhanced by non-coordinating anions, further proving that non-coordinating anion can be used in palladium-involved reactions.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Xiaoli Yu, Wei Yao, Huida Wan, Zhaojun Xu, Dawei Wang,