Synthesis of NN-diaryltoluene-4-sulphonamides

Ian G.C. Coutts; Michael Hamblin

doi:10.1039/P19750002445

Synthesis of NN-diaryltoluene-4-sulphonamides

Ian G.C. Coutts, Michael Hamblin

Nottingham Trent University

Research output: Contribution to journal › Article › peer-review

13 Citations (Scopus)

Abstract

The copper-catalysed reaction of N-arylsulphonamides with aryl bromides gives moderate to good yields of NN-diarylsulphonamides. The effect on yield of substituents is examined and the use of the synthesis as a route to unsymmetric diphenylamines is discussed.

Original language	English
Pages (from-to)	2445-2446
Number of pages	2
Journal	Journal of the Chemical Society, Perkin Transactions 1
Issue number	23
DOIs	https://doi.org/10.1039/P19750002445
Publication status	Published - 1975
Externally published	Yes

ASJC Scopus subject areas

General Chemistry

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10.1039/P19750002445

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title = "Synthesis of NN-diaryltoluene-4-sulphonamides",

abstract = "The copper-catalysed reaction of N-arylsulphonamides with aryl bromides gives moderate to good yields of NN-diarylsulphonamides. The effect on yield of substituents is examined and the use of the synthesis as a route to unsymmetric diphenylamines is discussed.",

author = "Coutts, \{Ian G.C.\} and Michael Hamblin",

year = "1975",

doi = "10.1039/P19750002445",

language = "English",

pages = "2445--2446",

journal = "Journal of the Chemical Society, Perkin Transactions 1",

issn = "1470-4358",

publisher = "Chemical Society",

number = "23",

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T1 - Synthesis of NN-diaryltoluene-4-sulphonamides

AU - Coutts, Ian G.C.

AU - Hamblin, Michael

PY - 1975

Y1 - 1975

N2 - The copper-catalysed reaction of N-arylsulphonamides with aryl bromides gives moderate to good yields of NN-diarylsulphonamides. The effect on yield of substituents is examined and the use of the synthesis as a route to unsymmetric diphenylamines is discussed.

AB - The copper-catalysed reaction of N-arylsulphonamides with aryl bromides gives moderate to good yields of NN-diarylsulphonamides. The effect on yield of substituents is examined and the use of the synthesis as a route to unsymmetric diphenylamines is discussed.

UR - https://www.scopus.com/pages/publications/37049130544

U2 - 10.1039/P19750002445

DO - 10.1039/P19750002445

M3 - Article

AN - SCOPUS:37049130544

SN - 1470-4358

SP - 2445

EP - 2446

JO - Journal of the Chemical Society, Perkin Transactions 1

JF - Journal of the Chemical Society, Perkin Transactions 1

IS - 23

ER -

Synthesis of NN-diaryltoluene-4-sulphonamides

Abstract

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