clozapine and 9-10-phenanthrenequinone

clozapine has been researched along with 9-10-phenanthrenequinone* in 1 studies

Other Studies

1 other study(ies) available for clozapine and 9-10-phenanthrenequinone

Article	Year
One-pot formation of 1,3,4-oxadiazol-2(3H)-ones and dibenzo[c,e]azepines by concomitant cathodic reduction of diazonium salts and phenanthrenequinones. The Journal of organic chemistry, 2013, Sep-20, Volume: 78, Issue:18 The one-pot concomitant electrochemical reduction of phenanthrenequinones (1, 2) and arenediazonium salts (3a-f) led to the formation of 1,3,4-oxadiazol-2(3H)-ones (4a-f, 5a) and dibenzo[c,e]azepines (6a-f) when N-methylformamide was used as the solvent. A new pathway, different from those previously described with other aprotic solvents, is proposed. The experimental data support a radical mechanism for the electrochemical process followed by an internal rearrangement to give the products. Topics: Clozapine; Diazonium Compounds; Electrodes; Molecular Structure; Oxadiazoles; Oxidation-Reduction; Phenanthrenes; Salts	2013

Article

Year

One-pot formation of 1,3,4-oxadiazol-2(3H)-ones and dibenzo[c,e]azepines by concomitant cathodic reduction of diazonium salts and phenanthrenequinones.

The Journal of organic chemistry, 2013, Sep-20, Volume: 78, Issue:18

The one-pot concomitant electrochemical reduction of phenanthrenequinones (1, 2) and arenediazonium salts (3a-f) led to the formation of 1,3,4-oxadiazol-2(3H)-ones (4a-f, 5a) and dibenzo[c,e]azepines (6a-f) when N-methylformamide was used as the solvent. A new pathway, different from those previously described with other aprotic solvents, is proposed. The experimental data support a radical mechanism for the electrochemical process followed by an internal rearrangement to give the products.

Topics: Clozapine; Diazonium Compounds; Electrodes; Molecular Structure; Oxadiazoles; Oxidation-Reduction; Phenanthrenes; Salts

2013