22156-88-3Relevant articles and documents
DMD Oxidation of in-Situ-Generated σH Adducts Derived from Nitroarenes and the Carbanion of 2-Phenylpropionitrile to Phenols: The First Direct Substitution of a Nitro by a Hydroxy Group
Adam, Waldemar,Ma?kosza, Mieczyslaw,Staliński, Krzysztof,Zhao, Cong-Gui
, p. 4390 - 4391 (2007/10/03)
The dimethyldioxirane (DMD) oxidation of σH adducts derived from nitroarenes and the carbanion of 2-phenyIpropionitrile yields unexpectedly the phenols 5 as the major products, while the usually observed nitroarenes 4 are formed in very little