J. Simonet, Hélène Dupuy
Jun 10, 1992
Citations
0
Influential Citations
3
Citations
Journal
Journal of Electroanalytical Chemistry
Abstract
Abstract Cathodically formed 1,4-diacetylbenzene dianion may react as a reducing species toward aromatic halides. It also reacts as an electrogenerated base with the starting product considered as a pronucleophile (source of enolate). The concomitant presence in solution of aromatic radicals and electrogenerated nucleophiles means that SRN1 type reactions may occur.