Enantioselective Synthesis of Quaternary α-Aminophosphonates via Conjugate Addition of α-Nitrophosphonates to Enones

Abstract

Enantioselective Michael addition of <b>α</b>-nitrophosphonates to enones for the synthesis of <b>α</b>-aminophosphonates is reported for the first time. The reaction proceeds in good to high yields and moderate to high selectivity in the presence of a new quinine thiourea catalyst. The quaternary nitrophosphonates were conveniently transformed to cyclic quaternary <b>α</b>-aminophosphonates via in situ reduction–intramolecular cyclization or Baeyer–Villiger oxidation followed by in situ reduction–intramolecular cyclization