Desymmetrizing Hydroformylation with the Aid of a Planar Chiral Catalyst-Directing Group
β Scribed by Breit, Bernhard; Breuninger, Daniel
- Book ID
- 119967599
- Publisher
- American Chemical Society
- Year
- 2004
- Tongue
- English
- Weight
- 58 KB
- Volume
- 126
- Category
- Article
- ISSN
- 0002-7863
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π SIMILAR VOLUMES
## Abstract The desymmetrizing hydroformylation of diallylcarbinols has been achieved by employing a planarβchiral, substrateβbound catalystβdirecting group β the __ortho__β(diphenylphosphanyl)ferrocenylcarbonyl group (__o__βDPPF). The method allows the simultaneous construction of two stereogenic
## Abstract For Abstract see ChemInform Abstract in Full Text.
Stereoselective hydroformylation and stereoselective conjugate addition to enoates has been achieved in a synthetic sequence employing a substrate-bound catalyst directing the o-DPPB group (o-DPPBsortho-diphenylphosphanyl benzoate). Furthermore, a stereoselective domino process combining hydroformyl