Although a naphthaquinone toluene-p-sulphonimide was hydrolysed by nitric acid to the 1,2-quinone, this reagent nitrated various N-toluene-p- sulphonylanisidines. Some of the sulphonylanisidines were converted into quinones by chromic acid but the sulphonamido-group remained intact during these reactions.
|Number of pages||4|
|Journal||Journal of the Chemical Society (Resumed)|
|Publication status||Published - 1960|