Kinetics of association between bisquaternary ammonium ligands and acetylcholinesterase. Evidence for two conformational states of the enzyme from stopped-flow measurements of fluorescence

Biochemistry ◽  
1979 ◽  
Vol 18 (16) ◽  
pp. 3622-3629 ◽  
Author(s):  
Michael B. Bolger ◽  
Palmer Taylor
1980 ◽  
Vol 103 (2) ◽  
pp. 313-321 ◽  
Author(s):  
Anita LANDSCHOOT ◽  
Frank G. LOONTIENS ◽  
Robert M. CLEGG ◽  
Thomas M. JOVIN

Langmuir ◽  
1998 ◽  
Vol 14 (3) ◽  
pp. 590-594 ◽  
Author(s):  
Samuel E. Campbell ◽  
Zhiqiang Zhang ◽  
Stig E. Friberg ◽  
Ramesh Patel

1986 ◽  
Vol 156 (2) ◽  
pp. 311-315 ◽  
Author(s):  
Jorg BAR ◽  
Gerhard HUBNER ◽  
Gerhard KOPPERSCHLAGER

2000 ◽  
Vol 29 (7) ◽  
pp. 487-498 ◽  
Author(s):  
E. Błachut-Okrasińska ◽  
E. Bojarska ◽  
A. Niedźwiecka ◽  
L. Chlebicka ◽  
E. Darżynkiewicz ◽  
...  

1966 ◽  
Vol 19 (8) ◽  
pp. 1365 ◽  
Author(s):  
RH Smith ◽  
IR Wilson

Initial rates of reaction for the above oxidation have been measured by a stopped-flow conductance method. Between pH 2 and 3.6, the initial rate of reaction, R, is given by the expression R{[HSO5-]+[SCN-]} = {kb+kc[H+]}[HSO5-]0[SCN-]20+ka[H+]-1[HSO5]20[SCN-]0 As pH increases, there is a transition to a pH-independent rate, first order in each thiocyanate and peroxomonosulphate concentrations.


Synthesis ◽  
2019 ◽  
Vol 51 (05) ◽  
pp. 1157-1170 ◽  
Author(s):  
Artem Leonov ◽  
Daria Timofeeva ◽  
Armin Ofial ◽  
Herbert Mayr

The kinetics of the reactions of trimethylsilyl enol ethers and enamines (derived from deoxybenzoin, indane-1-one, and α-tetralone) with reference electrophiles (p-quinone methides, benzhydrylium and indolylbenzylium ions) were measured by conventional and stopped-flow photometry in acetonitrile at 20 °C. The resulting second-order rate constants were subjected to a least-squares minimization based on the correlation equation lg k = s N(N + E) for determining the reactivity descriptors N and s N of the silyl enol ethers and enamines. The relative reactivities of structurally analogous silyl enol ethers, enamines, and enolate anions towards carbon-centered electrophiles are determined as 1, 107, and 1014, respectively. A survey of synthetic applications of enolate ions and their synthetic equivalents shows that their behavior can be properly described by their nucleophilicity parameters, which therefore can be used for designing novel synthetic transformations.


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