ChemInform Abstract: Asymmetric Hydroformylation of Conjugated Dienes Catalyzed by Chiral Phosphine-Phosphite-Rh(I) Complex.
β Scribed by T. HORIUCHI; T. OHTA; E. SHIRAKAWA; K. NOZAKI; H. TAKAYA
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 36 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Asymmetric Hydroformylation of Conjugated Dienes Catalyzed by Chiral Phosphine-Phosphite-Rh(I) Complex.
-Optically active Ξ²,Ξ³-unsaturated aldehydes are obtained in high regio-and enantioselectivities from dienes like (II) and (VI) by the title reaction with chiral (R,S)-BINAPHOS-Rh(I) complex as catalyst. Butadiene (IX) gives achiral products and (E)-and (Z)-pentadienes (XII) and (XIV) form the same major product (XIII) with low enantioselectivities. The reaction conditions are optimized by variation of the H2/CO pressure (1:1 mixtures) and the temperature. -(HORIUCHI,
π SIMILAR VOLUMES
## Mechanistic Aspects of Asymmetric Hydroformylation of Olefins Catalyzed by Chiral Phosphine-Phosphite-Rhodium(I) Complexes. -The effects of the partial pressure of CO (II) and H2 on the reaction rate and selectivity of the asymmetric hydroformylation of 1-hexene ( Ia) and styrene (Ib) are exam