42946-36-1Relevant articles and documents
The rate of cyclization of 2′- and 4′-substituted diphenylamine-2-carboxylic acids in sulfuric acid as a function of the electronic properties of substituents
Pelevin,Markovich,Nazarov,Galan,Kudryavtseva,Brylev
, p. 590 - 592 (2011)
The kinetic regularities of cyclization of 2′- and 4′-substituted diphenylamine-2-carboxylic acids in sulfuric acid were determined. The rate of cyclization of diphenylamine-2-carboxylic acids is linearly dependent on the nature of substituents in the meta-position relative to the reaction site in accordance with the two-parameter Hammett equation.
Nitric oxide releasing acridone carboxamide derivatives as reverters of doxorubicin resistance in MCF7/Dx cancer cells
Rajendra Prasad,Deepak Reddy,Kathmann, Ietje,Amareswararao,Peters
, p. 51 - 58 (2015/12/17)
A series of nitric oxide donating acridone derivatives are synthesized and evaluated for in vitro cytotoxic activity against different sensitive and resistant cancer cell lines MCF7/Wt, MCF7/Mr (BCRP overexpression) and MCF7/Dx (P-gp expression). The resu
Kinetic parameters of the intramolecular condensation of diphenylamine-2-carboxylic acid under microwave radiation
Markovich,Kudryavtseva,Brylev,Markovich,Koroleva
experimental part, p. 149 - 152 (2012/06/04)
The cyclization of diphenylamine-2-carboxylic acid under microwave radiation was investigated. The kinetic parameters of the processes were measured. The use of microwave radiation was found to reduce the reaction duration and to increase the target produ