Dissociation of aryl sulfonyl phthalimide radical anions: relevance to the biological activity of aryl sulfonyl amides.
Abdelaziz Houmam, Emad M Hamed
Index: Chem. Commun. (Camb.) 48(92) , 11328-30, (2012)
Full Text: HTML
Abstract
The reduction of two aryl sulfonyl phthalimides leads to the corresponding radical anions. Surprisingly, that of the nitro-derivative decomposes faster than that of the methyl derivative. A theoretical investigation along with application of the dissociative ET theory to the decomposition of radical anions allows rationalization of this unexpected behavior.
Related Compounds
Related Articles:
2013-01-01
[Bioorg. Med. Chem. Lett. 23(1) , 287-90, (2013)]
Phthalimido-ferrocidiphenol cyclodextrin complexes: Characterization and anticancer activity.
2015-08-01
[Int. J. Pharm. 491 , 323-34, (2015)]
2009-01-01
[Molecules 14(8) , 2976-84, (2009)]
2014-01-01
[J. AOAC Int. 97(4) , 965-77, (2014)]
Bioanalysis and enantioseparation of dl-carnitine in human plasma by the derivatization approach.
2015-10-01
[Bioanalysis 7 , 2477-88, (2015)]