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Novel oxidative rearrangement of β,γ-unsaturated ketone hydrazones on iodination in base
Authors:Michael E. Jung  Gregory L. Hatfield
Affiliation:Department of Chemistry, University of California, Los Angeles, California 90024 U.S.A.
Abstract:Iodination of the bicyclic enone hydrazone 3 in excess triethylamine gave, in addition to the expected vinyl iodide 4, the rearranged aromatic product 5.
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