Factors of chemical structure of arylselenides are considered in relation with their reactivity in the electrooxidation processes following stepwise or dissociative electron transfer (ET) mechanism. The reactivity of electrogenerated cation radicals (CRs) is determined by electronic and stereoelectronic effects affecting the charge distribution. Compensation of the charge on Se and lowering of the energy of the CRs favour the radical properties as compared to the ionic properties of these species. © 1998 OPA (Overseas Publishers Association) N. V. Published by license under the Gordon and Breach Science Publishers imprint
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Factors of chemical structure of arylselenides are considered in relation with their reactivity in t...
Factors of chemical structure of arylselenides are considered in relation with their reactivity in t...
Factors of chemical structure of arylselenides are considered in relation with their reactivity in t...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The oxidation of ring-substituted aryl(timethylsilylmethyl)sulfides and aryl(trimethylsilylmethyl)-s...
The oxidation of ring-substituted aryl(timethylsilylmethyl)sulfides and aryl(trimethylsilylmethyl)-s...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
The oxidation of ring-substituted aryl(timethylsilylmethyl)sulfides and aryl(trimethylsilylmethyl)-s...
The potential-determining reaction of cation radicals formed upon electrochemical oxidation of diphe...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Factors of chemical structure of arylselenides are considered in relation with their reactivity in t...
Factors of chemical structure of arylselenides are considered in relation with their reactivity in t...
Factors of chemical structure of arylselenides are considered in relation with their reactivity in t...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The role of stereoelectronic effects in the electrochemical oxidation of arylselenides Se-substitute...
The oxidation of ring-substituted aryl(timethylsilylmethyl)sulfides and aryl(trimethylsilylmethyl)-s...
The oxidation of ring-substituted aryl(timethylsilylmethyl)sulfides and aryl(trimethylsilylmethyl)-s...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
The oxidation of ring-substituted aryl(timethylsilylmethyl)sulfides and aryl(trimethylsilylmethyl)-s...
The potential-determining reaction of cation radicals formed upon electrochemical oxidation of diphe...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...
Electrochemical oxidation of arylmethylselenides in acetonitrile in the presence of a strong proton ...