156. Sulphonamides as a source of quinones

F. Bell

Research output: Contribution to journalArticlepeer-review


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 languageEnglish
Pages (from-to)769-772
Number of pages4
JournalJournal of the Chemical Society (Resumed)
Publication statusPublished - 1960


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