156. Sulphonamides as a source of quinones

F. Bell

Research output: Contribution to journalArticle

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

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sulfonamides
toluene
quinones
nitric acid
acids

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title = "156. Sulphonamides as a source of quinones",
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.",
author = "F. Bell",
year = "1960",
language = "English",
pages = "769--772",
journal = "Journal of the Chemical Society (Resumed)",
issn = "0368-1769",
publisher = "Chemical Society",

}

156. Sulphonamides as a source of quinones. / Bell, F.

In: Journal of the Chemical Society (Resumed), 1960, p. 769-772.

Research output: Contribution to journalArticle

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 -