123534-30-5Relevant academic research and scientific papers
Flow cell electrosynthesis of o-substituted nitrosobenzenes. In situ reaction with sulfinic acids. Attempt to prepare heterocycles.
Guilbaud-Criqui, A.,Moinet, C.
, p. 295 - 300 (2007/10/02)
Nitrosobenzenes with CO2H 1b, CO2CH3 2b, CONR2 3b-6b, CH2CO2H 7b, CHOHCO2H 8b and NHCO2CH3 9b ortho-substituted were prepared, in a "redox" cell, from the corresponding nitro compounds.Addition of sulfinic acids to the solution after electrolyses leads to
Electrochemistry of o-nitrosobenzoic acid in aqueous medium
Lamoureux, C.,Moinet, C.
, p. 599 - 603 (2007/10/02)
The electrosynthesis of 2-nitrosobenzoic acid from 2-nitrobenzoic acid, in a "redox" electrolysis cell with flowing solution through two consecutive porous working electrodes of opposite polarities, gives the monomeric form at the anode.An important part
REACTION OF ELECTROGENERATED 2-NITROSOBENZOIC ACIDS WITH SULPHINIC ACIDS. A CONVENIENT ROUTE TO N-SULFONYLBENZISOXAZOLONES
Gault, C.,Moinet, C.
, p. 3429 - 3436 (2007/10/02)
A one-pot synthesis of N-sulfonylbenzisoxazolones from 2-nitrobenzoic acids and sulphinic acids is described; it successively involves: - electrosynthesis, in a cell with two consecutive porous electrodes of opposite polarities, of the sodium salt of nitr
