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Kinetic studies on the homogeneous hydrogenation of fumaric and maleic acid catalysed by bis(dimethylglyoximato)cobalt(II)

TLDR
In this paper, the influence of varying concentrations of Co(dmgh)2, NaOH and axial base on the rate of hydrogenation of fumaric and maleic acids has been studied in detail.
Abstract
The influence of varying concentrations of Co(dmgh)2, NaOH and axial base on the rate of hydrogenation of fumaric and maleic acids has been studied in detail. Intramolecular hydrogen bonding in the monoanion of maleic acid and thetrans orientation of carboxylic acid groups in fumaric acid are important factors which account for the difference in the rate of hydrogenation of these substrates. Mono-, di-and trialkyl amines as axial bases modify the activity of the catalyst, dialkylamines conferring the maximum activity and trialkylamines the least. Back-strain on nitrogen atom and solvation energy of the amines are responsible for their different behaviours. A rate law has been proposed and verified

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References
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Journal ArticleDOI

New Developments in the Field of Vitamin B12: Enzymatic Reactions Dependent upon Corrins and Coenzyme B12

TL;DR: New ideas about the mode of action of vitamin B12 coenzymes in enzymatic reactions are focused on.
Journal ArticleDOI

Etude du mecanisme de l'hydrogenation des esters insatures catalysee par la vitamine B12 ou les cobaloximes

TL;DR: In this article, the mechanism of the hydrogenation of α, β-unsaturated esters by H 2 or NaBH 4 was studied. But the mechanism was not stereospecific, and a σ alkylcobalt complex was an intermediate.
Journal ArticleDOI

Asymmetric Reactions. IX. On the Catalytic Hydrogenation of Olefinic Compounds with Bis(dimethylglyoximato)cobalt(II)-base Complex

TL;DR: In this article, an analysis of the catalytic hydrogenation of twenty-one olefinic compounds with bis(dimethylglyoximato)cobalt(II)-pyridine complex with electron-withdrawing and a weakly electron-donating substituent is presented.
Journal ArticleDOI

Dichlorotris(triphenylphosphine)ruthenium(II) catalyzed dehydrogenation of some natural products using cyclohexanone as acceptor

TL;DR: Cyclohexanone has been used as an acceptor for the dehydrogenation of some natural products in the presence of RuCl2(PPh3)3 as mentioned in this paper.
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