A series of 1,4-dibenzyl-1,2,3,4-tetrahydroquinoxaline-6,7-dione derivatives (6a-6c) were electrosynthesized. In the present work, electrochemical oxidation of catechols 1a-1d in the presence of the N1,N2-dibenzylethane-1,2-diamine (3) as a nucleophile, has been studied in aqueous solutions using cyclic voltammetry and controlled-potential coulometry (CPC) methods. Various parameters such as the applied potential, pH of the electrolytic solution, cell configuration and also purification techniques, were carried out to optimize the yields of corresponding products. New quinoxaline-6,7-dione derivatives were synthesized in excellent yield using an electrochemical procedure coupled with a Schiff base as a facile, efficient and practical method
The detailed electrochemistry of a biologically active isoquinoline, 2-benzoyl-7-methoxy-2,3-dihydro...
The selective electrohydrogenation of nitro aliphatic and nitro aromatic functional groups in molecu...
The detailed electrochemistry of a biologically active isoquinoline, 2-benzoyl-7-methoxy-2,3-dihydro...
Electro-oxidation of catechol has been investigated in the absence of nucleophile. The studies were ...
Oxidation of hydroquinone (1a) has been studied in the presence of methyl cyanoacetate (3a) and ethy...
The main objective of this work is to synthesize of 4-nitrocatechol via a facile electrochemical met...
The electrochemical properties of 24 1,4-dioxidoquinoxalin-2-yl ketone derivatives with varying deg...
The project was concerned with the investigation of the electrochemical oxidation of various phenols...
The reactions of electrochemically generated o-quinones from oxidation of catechol and 4-methylcatec...
The oxidation of substituted catechols was studied by cyclic voltammetry, chronoamperometry, otatin...
The electrochemical behavior of three kinds of conjugated quinoxaline derivatives has been studied i...
4-substituted catechols are oxidized to the o- quinones which are unstable in aqueous solution . The...
In situ spectroelectrochemical detection of reaction intermediates was used as a decisive method for...
This study illustrates electrochemical behavior of hydroquinone and 4-amino-6-chlorobenzene-1,3-dis...
The electrochemical generation of o-quinone from catechol and its subsequent reaction with the some ...
The detailed electrochemistry of a biologically active isoquinoline, 2-benzoyl-7-methoxy-2,3-dihydro...
The selective electrohydrogenation of nitro aliphatic and nitro aromatic functional groups in molecu...
The detailed electrochemistry of a biologically active isoquinoline, 2-benzoyl-7-methoxy-2,3-dihydro...
Electro-oxidation of catechol has been investigated in the absence of nucleophile. The studies were ...
Oxidation of hydroquinone (1a) has been studied in the presence of methyl cyanoacetate (3a) and ethy...
The main objective of this work is to synthesize of 4-nitrocatechol via a facile electrochemical met...
The electrochemical properties of 24 1,4-dioxidoquinoxalin-2-yl ketone derivatives with varying deg...
The project was concerned with the investigation of the electrochemical oxidation of various phenols...
The reactions of electrochemically generated o-quinones from oxidation of catechol and 4-methylcatec...
The oxidation of substituted catechols was studied by cyclic voltammetry, chronoamperometry, otatin...
The electrochemical behavior of three kinds of conjugated quinoxaline derivatives has been studied i...
4-substituted catechols are oxidized to the o- quinones which are unstable in aqueous solution . The...
In situ spectroelectrochemical detection of reaction intermediates was used as a decisive method for...
This study illustrates electrochemical behavior of hydroquinone and 4-amino-6-chlorobenzene-1,3-dis...
The electrochemical generation of o-quinone from catechol and its subsequent reaction with the some ...
The detailed electrochemistry of a biologically active isoquinoline, 2-benzoyl-7-methoxy-2,3-dihydro...
The selective electrohydrogenation of nitro aliphatic and nitro aromatic functional groups in molecu...
The detailed electrochemistry of a biologically active isoquinoline, 2-benzoyl-7-methoxy-2,3-dihydro...