Résumé
Syntheses permitting the introduction of one or two methyl substituents at the sp3-hybridized carbon atom in the backbone of enantiopure 2-phospharuthenocenemethyl phosphines are presented. Preliminary Rh-catalyzed hydrogenations of enamides suggest that the interaction of the Cp* group with the side-arm methyl group lying endo to the phosphametallocene modifies enantioselectivity significantly with respect to the side-arm- unsubstituted analogue.
| langue originale | Anglais |
|---|---|
| Pages (de - à) | 1804-1811 |
| Nombre de pages | 8 |
| journal | Organometallics |
| Volume | 30 |
| Numéro de publication | 7 |
| Les DOIs | |
| état | Publié - 11 avr. 2011 |
| Modification externe | Oui |
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