Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1346603 | Tetrahedron: Asymmetry | 2012 | 4 Pages |
PEG-400-H2O was found to be a green and recyclable reaction medium for asymmetric hydrogenations of aromatic ketones catalyzed by a ruthenium achiral monophosphine complex RuCl2(TPPTS)2 [TPPTS: P(m-C6H4SO3Na)3] modified by (S,S)-DPENDS [disodium salt of sulfonated (S,S)-1,2-diphenyl-1,2-ethylene-diamine]. The acetophenone product was obtained with 86.3% ee under the optimized conditions. The resulting products can be easily separated from the catalyst by extraction with n-hexane. The catalyst immobilized in PEG-400-H2O not only exhibits excellent activity and enantioselectivity, but also can be recycled and reused several times without a loss of activity or enantioselectivity.
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