Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5275949 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
An investigation of the utility of N-sulfonyloxaziridines to effect the oxidative rearrangement of tetrahydrobenzimidazoles to spiro fused 5-imidazolones is reported. In addition to the anticipated rearrangement manifold, it was found that 2-amino substituted derivatives afford products resulting from rearrangement, or alternatively from addition of methanol or water depending on the nature of the N-substituents and reaction conditions.
Graphical abstractTreatment of tetrahydrobenzimidazoles with N-sulfonyloxaziridines leads to the formation of spiro fused 5-imidazolone in moderate to excellent yield.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Rasapalli Sivappa, Panduka Koswatta, Carl J. Lovely,