[摘要]:The catalytic asymmetric Friedel-Crafts/protonation of indoles and pyrroles with a-substituted nitroalkenes to give the corresponding adducts in a highly anti-selective manner was achieved by an imidazoline aminophenol (L2)-Cu complex. The anti-adducts could be successfully transformed to biochemically important alpha-substituted beta-heteroarylalkylamines. |