Highly enantioselective borohydride reductions of 2-phenacylpyridine catalyzed by optically active β-ketoiminato cobalt(II) complexes
- 1 September 2000
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 11 (18) , 3671-3674
- https://doi.org/10.1016/s0957-4166(00)00369-4
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- A concise synthesis of homochiral sedamines and related alkaloids. A new reductive application of Jacobsen's catalystTetrahedron Letters, 1999
- Four-Coordinate Dimethylgallium Compounds Vary in Stability toward HydrolysisOrganometallics, 1998
- New and efficient catalysts for enantioselective borohydride reduction of ketones and iminesCatalysis Surveys from Japan, 1998
- Enantioselective Borohydride Reduction of N-Diphenylphosphinyl Imines Using Optically Active Cobalt(II) Complex CatalystsChemistry Letters, 1997
- Effects of Ligands and Additive Alcohols on Enantioselection in Highly Efficient Asymmetric Borohydride Reduction of Ketones Catalyzed by Optically Active Aldiminato Cobalt(II) ComplexesSynlett, 1996
- Preferential hydrogenation of aldehydes and ketones.Journal of the American Chemical Society, 1995
- Optically active β-ketoiminato manganese(III) complexes as efficient catalysts in enantioselective aerobic epoxidation of unfunctionalized olefinsInorganica Chimica Acta, 1994