## Abstract The title reaction affords high enantiomeric excesses but also a high substrate dependence is observed.
Iridium-catalyzed asymmetric hydrogenation of olefins using TIQ phosphine–oxazoline ligands
✍ Scribed by Sai Kumar Chakka; Byron K. Peters; Pher G. Andersson; Glenn E.M. Maguire; Hendrik G. Kruger; Thavendran Govender
- Book ID
- 108284624
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 904 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0957-4166
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📜 SIMILAR VOLUMES
The synthesis of a series of phosphine-oxazoline ligands is reported. This ligands are synthesized by reaction of a phosphine chloride with the secondary nitrogen of proline. Upon coordination to iridium the resulting complexes can be used in the asymmetric hydrogenation of simple olefins. The effec
## Abstract Herein we describe the synthesis of a new class of chiral phosphine‐oxazolines and their application as ligands in iridium‐catalyzed hydrogenations. Mechanistic aspects of olefin hydrogenation with this class of iridium catalysts are discussed and a selectivity model to help rationalize