Abstract
AbstractA series of 1‐substituted 1,2,3,4‐tetrahydroisoquinolines is prepared by oxidation of substrates (I) with bis(trifluoroacetoxy)iodobenzene followed by coupling of the intermediate iminium cation with a nucleophile, e.g. phthalimide, p‐toluenesulfonamide, or a Grignard reagent.
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