Synthesis of α-Amino Phosphonates Under Diastereocontrol by Imidazolidin-2-One Auxiliaries
- 1 October 1998
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 28 (20) , 3877-3884
- https://doi.org/10.1080/00397919808004941
Abstract
Ephedrine derived (4R,5S)-imidazolidin-2-one auxiliaries demonstrate phenomenal diastereocontrol in the addition of phosphite to chiral imine derivatives.Keywords
This publication has 5 references indexed in Scilit:
- Asymmetric synthesis of α-aminophosphonates via diastereoselective addition of phosphite to chiral imine derivativesTetrahedron: Asymmetry, 1996
- Enantioselective Synthesis of Diverse .alpha.-Amino Phosphonate DiestersJournal of the American Chemical Society, 1995
- Ephedrine‐Derived Imidazolidin‐2‐ones. Broad Utility Chiral Auxiliaries in Asymmetric SynthesisEuropean Journal of Inorganic Chemistry, 1993
- A novel imidazolidin-2-one auxiliary for a highly stereoselective aldol route to β-hydroxyesters.Tetrahedron: Asymmetry, 1992
- Asymmetric diels-alder reactions : facile preparation and structure of sulfonamido-isobornyl acrylatesTetrahedron Letters, 1984