Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5286135 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
The interaction of N-(1-aryl-2,2,2-trichloroethyl)amides of arenesulfonic acids with secondary amines or their salts in the presence of inorganic bases involves the formation of chloroaziridine intermediates. Depending upon the solvent and reagent ratio, the reaction results in N-[1-dialkylamino-2-chloro-2-arylethylidene]-, N-[2-dialkylamino-1-chloro-2-arylethylidene]-, N-[1,2-bis(dialkylamino)-2-arylethylidene]-, and N-(1,2-dioxo-2-arylethene)amides of arenesulfonic acids.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Igor B. Rozentsveig, Galina G. Levkovskaya, Gulnur N. Rozentsveig, Anna N. Mirskova, Leonid B. Krivdin, Ludmila I. Larina, Aleksandr I. Albanov,