Asymmetric hydrogenation of α-ethylstyrenes catalyzed by chiral ruthenium complexes
✍ Scribed by Grant S Forman; Takeshi Ohkuma; William P Hems; Ryoji Noyori
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 66 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A combined system of RuCl 2 (R,R)-Me-DuPhos n and t-C 4 H 9 OK catalyzes the asymmetric hydrogenation of a-ethylstyrene derivatives. The reaction proceeds with a substrate to catalyst molar ratio of up to 2600 in 2-propanol at 8 atm and room temperature to give the chiral saturated products in 81-89% ee.
📜 SIMILAR VOLUMES
Chiral ruthenium hydrides : HRuCl(TRPC)2 and H2Ru(TBPC)2 catalyse the hydrogenation of a-&unsaturated ketones to ketones (e.e. 62 X). Asymmetric hydrogenation of prochiral olefins in the presence of chiral rhodium catalyst 1 is now a useful preparative tool for many a-aminoacids