Abstract
Four tetranuclear ruthenium carbonyl hydrido clusters consisting of the enantiomeric pairs [H4Ru4(CO)10{-1,2-(R/S,R/S)-bdpp}] and [H4Ru4(CO)10{1,1-(R/S,R/S)-bdpp}] containing chiral (R,R)- or (S,S)-bdpp [bdpp = (2R/S,4R/S)-2,4-bis(diphenylphosphino)pentane] have been prepared and fully characterized. These clusters catalyze asymmetric hydrogenation of tiglic acid [trans-2-methyl-2-butenoic acid] with high conversion rates (75-100%) under relatively mild reaction conditions. Enantiomeric excesses of 40-46% were observed; the predominating enantiomeric form of the hydrogenated product is dependent on the configuration of the diphosphine ligand, indicating strong chiral induction.
| Original language | English |
|---|---|
| Pages (from-to) | 5568 |
| Journal | Organometallics |
| Volume | 19 |
| Issue number | 26 |
| DOIs | |
| Publication status | Published - 2000 |
Subject classification (UKÄ)
- Inorganic Chemistry
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