Synthesis of β-alkoxy-N-protected phenethylamines via one-pot copper-catalyzed aziridination and ring opening

A regioselective, copper-catalyzed, one-pot aminoalkoxylation of styrenes using primary and secondary alcohols and three different iminoiodanes as alkoxy and nitrogen sources respectively, is reported. The beta-alkoxy-N-protected phenethylamines obtained were used to synthesise beta-alkoxy-N-benzylphenethylamines which are interesting new compounds that could act as possible neuronal ligands.