Lipase/Palladium-Catalyzed Asymmetric Transformations of Ketoximes to Optically Active Amines
- 16 November 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 3 (25), 4099-4101
- https://doi.org/10.1021/ol0168622
Abstract
Prochiral ketoximes were asymmetrically transformed to optically active amines in the acetylated forms by coupled lipase/palladium catalysis in the presence of an acyl donor under 1 atm of hydrogen.Keywords
This publication has 19 references indexed in Scilit:
- Studies on the asymmetric reduction of β-oximino methyl ether boronates: reagent control, double diastereocontrol and transmitted remote asymmetric inductionJournal of the Chemical Society, Perkin Transactions 1, 2000
- Enantioselective Reduction of Oxime Ethers with Borane Catalyzed by Polymer-Supported 2-PiperazinemethanolThe Journal of Organic Chemistry, 2000
- Ruthenium-mediated reduction of oximes to imines. Synthesis, characterization and redox properties of imine complexes of rutheniumJ. Chem. Soc., Dalton Trans., 2000
- Concerted Catalytic Reactions for Conversion of Ketones or Enol Acetates to Chiral AcetatesOrganic Letters, 2000
- Iridium-Catalyzed Enantioselective Hydrogenation of Imines in Supercritical Carbon DioxideJournal of the American Chemical Society, 1999
- Iridium-Catalyzed Asymmetric Hydrosilylation of Imines Using Chiral Oxazolinyl-Phosphine LigandsOrganometallics, 1999
- Asymmetric Rh-Catalyzed Hydrogenation of Enamides with a Chiral 1,4-Bisphosphine Bearing Diphenylphosphino GroupsThe Journal of Organic Chemistry, 1998
- A Convenient Asymmetric Synthesis of α-1-Arylalkylamines through the Enantioselective Hydrogenation of EnamidesJournal of the American Chemical Society, 1996
- The ruthenium catalyzed asymmetric hydrogenation of oximes using binap as the chiral ligandTetrahedron: Asymmetry, 1992
- Enantioselective Catalytic Hydrosilylation of OximesAngewandte Chemie International Edition in English, 1984