Nosylaziridines are highly reactive electrophiles towards a variety of nucleophiles yielding the corresponding SN2 adducts without competing attack on the nosyl functionality (SNAr). The resulting primary nosylamide adducts can be readily cleaved under mild conditions to provide the primary amines. (C) 1997 Elsevier Science Ltd.
Synthesis of β-alkoxy-<i>N</i>-protected phenethylamines <i>via</i> one-pot copper-catalyzed aziridination and ring opening
作者:Jorge Saavedra-Olavarría、Matías Madrid-Rojas、Iriux Almodovar、Patricio Hermosilla-Ibáñez、Edwin G. Pérez
DOI:10.1039/c8ra03815e
日期:——
one-pot aminoalkoxylation of styrenes using primary and secondary alcohols and three different iminoiodanes as alkoxy and nitrogen sources respectively, is reported. The β-alkoxy-N-protected phenethylamines obtained were used to synthesise β-alkoxy-N-benzylphenethylamines which are interesting new compounds that could act as possible neuronal ligands.