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Oxidative rearrangements of arylalkenes with [hydroxy(tosyloxy)iodo]benzene in 95% methanol: a general, regiospecific synthesis of α-aryl ketones
Authors:Michael W. Justik
Affiliation:Department of Chemistry, The University of Akron, Akron, OH 44325-3601, USA
Abstract:
The treatment of arylalkenes with [hydroxy(tosyloxy)iodo]benzene in 95% methanol affords the corresponding α-aryl ketones. This oxidative rearrangement is general for acyclic and cyclic arylalkenes and permits regioselective syntheses of isomeric α-phenyl ketone pairs.
Keywords:Oxidative rearrangement   Hypervalent iodine
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