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Journal ArticleDOI

Mechanistic aspects of catalytic hydrogenation of ketones by rhodium(I)-peralkyldiphosphine complexes

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TLDR
In this article, a general reaction scheme was proposed for the hydrogenation of ketones employing cationic rhodium(I) complexes and a neutral complex, which showed an unusual negative temperature dependence of the reaction rate.
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This article is published in Journal of Organometallic Chemistry.The article was published on 1985-01-08. It has received 47 citations till now. The article focuses on the topics: Norbornadiene & Acetophenone.

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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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The Metal−Ligand Bifunctional Catalysis: A Theoretical Study on the Ruthenium(II)-Catalyzed Hydrogen Transfer between Alcohols and Carbonyl Compounds

TL;DR: The ternary system consisting of [RuCl2(η6-benzene)]2, N-tosylethylenediamine or ethanolamine, and KOH (Ru:amine:KOH = 1:1:2 molar ratio) catalyzes reversible hydrogen transfer between alcohols and carbonyl compounds.
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Asymmetric synthesis. Practical production of D and L threonine. Dynamic kinetic resolution in rhodium and ruthenium catalyzed hydrogenation of 2-acylamino-3-oxobutyrates.

TL;DR: In this paper, an anti-selective synthesis of D and L threonine using chiral P * P Rh (I) 8 and Ru (II) 10 catalysts was described.
References
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Stereochemistry of reaction paths at carbonyl centres

TL;DR: In this article, the reaction paths found by different methods for different nucleophiles show some striking similarities that appear to be characteristic for the reaction type, and the results of recent experimental and theoretical studies of nucleophilic addition to carbonyl groups are described.
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