Vicinal Substituted Resorcinols. III. Extension of the Reaction between m-Dinitrobenzene, Potassium Cyanide and Methanol to Other Alcohols. The Mechanism of the Reaction

1943 ◽  
Vol 65 (12) ◽  
pp. 2379-2380 ◽  
Author(s):  
Alfred Russell ◽  
L. M. Addison
Keyword(s):  
Potassium Cyanide ◽  
Mechanism Of The Reaction

Mechanism of the reaction of 1-tert-butyl-3-azetidinyl tosylate with methanolic potassium cyanide and with solvent

1972 ◽  
Vol 37 (3) ◽  
pp. 524-526 ◽  
Author(s):  
Robert H. Higgins ◽  
Fred M. Behlen ◽  
Douglas F. Eggli ◽  
James H. Kreymborg ◽  
Norman H. Cromwell
Keyword(s):  
Potassium Cyanide ◽  
Tert Butyl ◽  
Mechanism Of The Reaction

Dependence of Platelet Adenyl Cyclase System on Oxidative Phosphorylation

1975 ◽  
Vol 34 (01) ◽  
pp. 042-049 ◽  
Author(s):  
Shuichi Hashimoto ◽  
Sachiko Shibata ◽  
Bokro Kobayashi
Keyword(s):  
Cyclic Amp ◽  
Oxidative Phosphorylation ◽  
Sodium Succinate ◽  
Potassium Cyanide ◽  
Adenyl Cyclase ◽  
Mitochondrial Oxidative Phosphorylation ◽  
Adenyl Cyclase Activity ◽  
Intact Rabbit ◽  
Adenyl Cyclase System ◽  
Cyclic Amp Synthesis

SummaryThe radioactive adenosine 3′,5′-monophosphate (cyclic AMP) level derived from 8-14C adenine in intact rabbit platelets decreased in the presence of mitochondrial inhibitor (potassium cyanide) or uncoupler (sodium azide), and markedly increased by the addition of NaF, monoiodoacetic acid (MIA), or 2-deoxy-D-glucose. The stimulative effect of the glycolytic inhibitors was distinctly enhanced by the simultaneous addition of sodium succinate. MIA did neither directly stimulate the adenyl cyclase activity nor inhibit the phosphodiesterase activity. These results suggest that cyclic AMP synthesis in platelets is closely linked to mitochondrial oxidative phosphorylation.

Acetolysis of 4β-methanesulphonyloxy-6β,7aβ-cyclo-B-homo-5α-cholestane

1979 ◽  
Vol 44 (11) ◽  
pp. 3308-3320 ◽  
Author(s):  
Ladislav Kohout ◽  
Jan Fajkoš
Keyword(s):  
Mechanism Of The Reaction

Synthesis of 4β-methanesulphonyloxy-6β,7aβ-cyclo-B-homo-5α-cholestane is described. During its acetolysis a kind of conjugative stabilization of the carbocation formed was observed. The mechanism of the reaction is discussed.

Kinetics and mechanism of the reaction of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione

1990 ◽  
Vol 55 (8) ◽  
pp. 1984-1990 ◽  
Author(s):  
José M. Hernando ◽  
Olimpio Montero ◽  
Carlos Blanco
Keyword(s):  
Aqueous Solution ◽  
Metal Ion ◽  
Activation Parameters ◽  
Enol Form ◽  
Kinetics And Mechanism ◽  
Kinetic Constants ◽  
Steric Factors ◽  
Kinetics Of ◽  
Mechanism Of The Reaction

The kinetics of the reactions of iron(III) with 6-methyl-2,4-heptanedione and 3,5-heptanedione to form the corresponding monocomplexes have been studied spectrophotometrically in the range 5 °C to 16 °C at I 25 mol l-1 in aqueous solution. In the proposed mechanism for the two complexes, the enol form reacts with the metal ion by parallel acid-independent and inverse-acid paths. The kinetic constants for both pathways have been calculated at five temperatures. Activation parameters have also been calculated. The results are consistent with an associative activation for Fe(H2O)63+ and dissociative activation for Fe(H2O)5(OH)2+. The differences in the results for the complexes of heptanediones studied are interpreted in terms of steric factors.

Kinetics and mechanism of the reaction between oxidized cytochrome c and ascorbic acid

1991 ◽  
Vol 56 (2) ◽  
pp. 478-490 ◽  
Author(s):  
Joaquin F. Perez-Benito ◽  
Conchita Arias
Keyword(s):  
Ascorbic Acid ◽  
Cytochrome C ◽  
Redox Reactions ◽  
Arrhenius Equation ◽  
Horse Heart Cytochrome ◽  
First Order ◽  
Acidic Form ◽  
Ph Range ◽  
Horse Heart Cytochrome C ◽  
Mechanism Of The Reaction

The reaction between horse-heart cytochrome c and ascorbic acid has been investigated in the pH range 5.5 – 7.1 and at 10.0 – 25.0 °C. The rate shows a first-order dependence on the concentration of cytochrome c, it increases in a non-linear way as the concentration of ascorbic acid increases, it increases markedly with increasing pH and, provided that the ionic strength of the medium is high enough, it fulfills the Arrhenius equation. The apparent activation energy increases as the pH of the solution increases. The results have been explained by means of a mechanism that includes the existence of an equilibrium between two forms (acidic and basic) of oxidized cytochrome c: cyt-H+ -Fe3+ + OH- cyt -Fe3+ + H2O, whose equilibrium constant is (6.7 ± 1.4). 108 at 25.0 °C, the acidic form being more reducible than the basic one. It is suggested that there is a linkage of hydrogenascorbate ion to both forms of cytochrome c previous to the redox reactions. Two possibilities for the oxidant-reductant linkage (binding and adsorption) are discussed in detail.

scholarly journals ON THE MECHANISM OF THE REACTION OF NINHYDRIN WITH α-AMINO ACIDS

1950 ◽  
Vol 186 (1) ◽  
pp. 13-22
Author(s):  
Douglas A. MacFadyen ◽  
Nathalie. Fowler
Keyword(s):  
Amino Acids ◽  
Mechanism Of The Reaction

Preparation of fluoroperoxytrifluoromethane. Mechanism of the reaction of oxygen difluoride and carbonyl fluoride

1972 ◽  
Vol 11 (1) ◽  
pp. 195-196 ◽  
Author(s):  
I. J. Solomon ◽  
A. J. Kacmarek ◽  
W. K. Sumida ◽  
J. K. Raney
Keyword(s):  
Mechanism Of The Reaction ◽  
Carbonyl Fluoride
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