[GRAPHICS]
Beckmann rearrangement of oxime is catalyzed by [RhCl(cod)](2), trifluorome
thanesulfonic acid, and tris(p-tolyl)phosphine in refluxing dichloroethane,
giving the corresponding amide in good yield. Product/acid ratios of 10:20
can be attained in the reaction of benzophenone oximes.