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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156. Sulphonamides as a source of quinones. / Bell, F.
In: Journal of the Chemical Society (Resumed), 1960, p. 769-772.Research output: Contribution to journal › Article
TY - JOUR
T1 - 156. Sulphonamides as a source of quinones
AU - Bell, F.
PY - 1960
Y1 - 1960
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=37049063175&partnerID=8YFLogxK
M3 - Article
SP - 769
EP - 772
JO - Journal of the Chemical Society (Resumed)
JF - Journal of the Chemical Society (Resumed)
SN - 0368-1769
ER -