New Ruthenium Catalysts for Asymmetric Transfer Hydrogenation of Prochiral Ketones
โ Scribed by Stephan Enthaler; Bernhard Hagemann; Santosh Bhor; Gopinathan Anilkumar; Man Kin Tse; Bianca Bitterlich; Kathrin Junge; Giulia Erre; Matthias Beller
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 139 KB
- Volume
- 349
- Category
- Article
- ISSN
- 1615-4150
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โฆ Synopsis
Abstract
Tridentate N,N,Nโpyridinebisimidazolines have been studied as new ligands for the enantioselective transfer hydrogenation of prochiral ketones. High yields and excellent enantioselectivity up to >99โ% ee have been achieved with an in situ generated catalytic system containing dichlorotris(triphenylphosphine)ruthenium and 2,6โbisโ([4R,5R]โ4,5โdiphenylโ4,5โdihydroโ1__H__โimidazolโ2โyl)โpyridine (3a) in the presence of sodium isopropoxide.
๐ SIMILAR VOLUMES
The nature of ruthenium-amino alcohol precursors in the aminoethane (1) coordinates through two nitrogen atoms, was structurally characterised by X-ray diffraction (8). -catalytic cycle of asymmetric hydrogen transfer reactions was studied using two C 2 -symmetrical tetradentate ligands (1 and Based
## Abstract The osmium compound __trans__,__cis__โ[OsCl~2~(PPh~3~)~2~(Pyme)] (1) (Pyme=1โ(pyridinโ2โyl)methanamine), obtained from [OsCl~2~(PPh~3~)~3~] and Pyme, thermally isomerizes to __cis__,__cis__โ[OsCl~2~(PPh~3~)~2~(Pyme)] (2) in mesitylene at 150โยฐC. Reaction of [OsCl~2~(PPh~3~)~3~] with Ph~