New chiral phosphinamide catalysts for highly enantioselective reduction of ketones
- 15 April 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (16) , 2853-2856
- https://doi.org/10.1016/0040-4039(96)00404-2
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Enantioselective reduction of ketones by borane catalysed by oxazaphospholidine oxidesTetrahedron Letters, 1996
- Stereoelectronic requirements for a new class of asymmetric ketone reduction catalysts containing an NPO structural unit.Tetrahedron: Asymmetry, 1994
- Direct preparation of N-diphenylphosphinoyl aziridines from 1,2-aminoalcohols utilizing nucleofugacity of diphenylphosphinatesTetrahedron Letters, 1994
- The Synthesis and Reactivity ofN-Diphenylphosphinyl AziridinesSynlett, 1994
- New catalysts containing an N-PO structural unit for the asymmetric reduction of ketones.Tetrahedron Letters, 1993
- Enantioselective reduction of ketones with borane, catalyzed by (S)-(−)-proline or (S)-(+)-prolinol.Tetrahedron: Asymmetry, 1993
- Enantioselective Borane Reduction of Ketones Catalyzed by a Chiral Oxazaphospholidine Borane ComplexPhosphorus, Sulfur, and Silicon and the Related Elements, 1993
- Enantioselective borane reduction of ketones catalysed by a chiral oxazaphospholidine–borane complexJournal of the Chemical Society, Chemical Communications, 1992
- The nucleophilic displacement route to homochiral arylphosphine oxidesTetrahedron, 1990