| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1325510 | Journal of Organometallic Chemistry | 2008 | 4 Pages |
Abstract
The versatility of the palladium(II) chloride and triethylsilane system has been tested in the reduction of aromatic carbonyl compounds. The reaction takes place under mild conditions. This facile and efficient method affords high yields for the reduction of aldehydes and ketones to the corresponding alkanes.
Graphical abstractThe versatility of the palladium(II) chloride and triethylsilane system has been tested in the reduction of aromatic carbonyl compounds. The reaction takes place under mild conditions and affords high yields. This facile and efficient method affords high yields for the reduction of aldehydes and Ketones to the corresponding alkanes.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Maryam Mirza-Aghayan, Rabah Boukherroub, Mahshid Rahimifard,