Asymmetric Isothiourea-Catalysed Formal [3+2] Cycloadditions of Ammonium Enolates with Oxaziridines

Chemistry. 2015 Jul 13;21(29):10530-6. doi: 10.1002/chem.201501271. Epub 2015 Jun 12.

Abstract

A highly enantioselective Lewis base-catalysed formal [3+2] cycloaddition of ammonium enolates and oxaziridines to give stereodefined oxazolidin-4-ones in high yield is described. Employing an enantioenriched oxaziridine in this process leads to a matched/mis-matched effect with the isothiourea catalyst and allowed the synthesis of either syn- or anti-stereodefined oxazolidin-4-ones in high d.r., yield and ee. Additionally, the oxazolidin-4-one products have been derivatised to afford functionalised enantioenriched building blocks.

Keywords: Lewis base; asymmetric synthesis; heterocycles; organocatalysis; oxaziridines.

Publication types

  • Research Support, Non-U.S. Gov't