| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 190796 | Electrochimica Acta | 2011 | 4 Pages |
Abstract
Simultaneous double electro-induced synthesis of Michael adducts in both the compartments of a divided cell has been achieved by galvanostatic electrolysis in 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid, exploiting the direct electro-generation of the enolate in the cathodic side and the electro-generation of the Lewis acid BF3 in the anodic side of the cell.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Linear paired electrolysis for C–C bond formation by Michael reaction. ► Exploitation of EMImBF4 ionic liquid as solvent/electrolyte system and pre-catalyst. ► Electrogenerated BF3 as catalyst.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Laura Palombi,