Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 769-772 |
| Number of pages | 4 |
| Journal | Journal of the Chemical Society (Resumed) |
| Publication status | Published - 1960 |
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Cite this
Bell, F. (1960). 156. Sulphonamides as a source of quinones. Journal of the Chemical Society (Resumed), 769-772.