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Ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation of Ketones Using a Formic Acid−Triethylamine Mixture

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This article is published in Journal of the American Chemical Society.The article was published on 1996-03-13. It has received 995 citations till now. The article focuses on the topics: Transfer hydrogenation & Formic acid.

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Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo‐ and Stereoselective Hydrogenation of Ketones

TL;DR: The newly devised [RuCl(2)(phosphane)(2)(1,2-diamine)] complexes are excellent precatalysts for homogeneous hydrogenation of simple ketones which lack any functionality capable of interacting with the metal center.
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Catalytic activities of Schiff base transition metal complexes

TL;DR: A review of the catalytic activity of metal complexes of binaphthyl compounds and their combinations with salen Schiff base is presented in this paper, where the pyridyl bis (imide) and pyridine bis(imine) complexes of cobalt(II), iron(II) ions have been used as catalysts in the polymerization of ethylene and propylene.
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Mechanisms of the H2-hydrogenation and transfer hydrogenation of polar bonds catalyzed by ruthenium hydride complexes

TL;DR: In this article, the authors classified the catalytic cycles for the H2-hydrogenation (H) and transfer hydrogenation (T) of CO and cN bonds catalyzed by over 100 ruthenium hydride complexes in organic and aqueous media.
References
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Journal ArticleDOI

Asymmetric catalytic reduction of carbonyl compounds using C2 symmetric diamines as chiral ligands

TL;DR: In this paper, the catalytic asymmetric reduction of prochiral ketones by hydride transfer using various C 2 symmetric chiral diamines as ligands and rhodium complexes is studied.
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Enantioselective catalytic reduction of ketones using C2-symmetric diamines as chiral ligands

TL;DR: In this article, the catalytic enantioselective reduction of various prochiral ketones using C 2 -symmetric diamines as ligands was reported, and up to 99% e.g. at 100% conversion are obtained.
Journal ArticleDOI

Chlorosulfenylated Carbonic Acid Derivatives

G. Zumach, +1 more
- 01 Jan 1970 - 
TL;DR: In this paper, the synthesis of chlorocarbonylsulfenyl chloride and its imino analogs is discussed, and the chemical behavior of these bifunctional compounds is illustrated for selected examples.
Journal ArticleDOI

Schiff bases as added chiral ligands for the [Ru(η6-C6H6)Cl2]2 catalysed hydrogen-transfer reduction of ketones with 2-propanol

TL;DR: Ruthenium complexes generated in situ from [Ru(C6H6)Cl2]2 and chiral Schiff bases [derived from(1R,2R)-diaminocyclohexane] catalyse asymmetric hydrogen-transfer reduction of alkyl aryl ketones by 2-propanol to give the (S)-alcohol in up to 40% ee.
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