| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1324857 | Journal of Organometallic Chemistry | 2011 | 4 Pages |
Abstract
Palladium-catalyzed inter- and intramolecular hydroaminations of styrenes that are coupled to alcohol oxidation under oxidative condition are reported. The fluorination reagent NFSI is used as the nitrogen source as well as the oxidant. Bidental nitrogen ligand bathocuproine plays a crucial role in this transformation.
Graphical abstractPalladium-catalyzed inter- and intramolecular hydroaminations of styrenes that are coupled to alcohol oxidation under oxidative condition are reported. The fluorination reagent NFSI is used as the nitrogen source as well as the oxidant. Bidental nitrogen ligand bathocuproine plays a crucial role in this transformation.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
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Authors
Tao Xu, Shuifa Qiu, Guosheng Liu,