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A new asymmetric synthesis of trans-hydroisoquinolones
Authors:Kamatani A  Overman L E
Institution:Department of Chemistry, 516 Rowland Hall, University of California, Irvine, California 92697-2025, USA.
Abstract:reaction: see text]. A convenient enantioselective synthesis of trans-hydroisoquinolones is described. This synthesis capitalizes on the ready availability of enantioenriched 2-substituted cyclohexenols by exploiting the asymmetry of an allylic carbon-oxygen sigma bond to control carbon-carbon bond formation in pinacol-terminated cyclizations of N-acyliminium cations.
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