The Enantioselective Dehydrogenation of Racemic Secondary Alcohols Catalyzed by Dimeric Ruthenium(II) Chiral Diphosphine Complexes
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/51/10/51_10_2807/_pdf
Reference40 articles.
1. Asymmetric Catalytic Hydrogenation with an Optically Active Phosphinerhodium Complex in Homogeneous Solution
2. Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphine
3. Hydrogenation of organic compounds using homogeneous catalysts
4. Asymmetric hydrogenation with a complex of rhodium and a chiral bisphosphine
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1. Asymmetric hydrogen transfer reactions promoted by homogeneous transition metal catalysts;Chemical Reviews;1992-07
2. Regio- and stereoselective dehydrogenation of .alpha.,.omega.-diols catalyzed by a rhodium hydride complex;The Journal of Organic Chemistry;1986-07
3. Ruthenium complex-catalyzed enantiotopos-differentiating dehydrogenation from diols.;NIPPON KAGAKU KAISHI;1985
4. A kinetic study on asymmetric transfer hydrogenation of unsaturated acids and esters by alcohols with binuclear ruthenium(II) chiral diphosphine complexes;Journal of the Chemical Society, Perkin Transactions 2;1984
5. Mechanistic investigation of homogeneous hydrogen transfer from 1-phenylethanol to cyclohexanone catalyzed by dichlorotris(triphenylphosphine)- ruthenium(II);Journal of Molecular Catalysis;1983-08
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