Chlorosulfonation of N-arylmaleimides

Article abstract of DOI:10.1080/10426509308034412

N-phenylmaleimides, o-, m- and p-substituted (1) reacted with excess chlorosulfonic acid to give the corresponding sulphonyl chlorides (2-5). These were condensed with amines and phenols to give derivatives (7-29) which underwent hydrolysis or ammonolysis

Full text of DOI:10.1080/10426509308034412

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Phosphorus, Sulfur, and Silicon and the
Related Elements
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CHLOROSULFONATION OF N-
ARYLMALEIMIDES
Augusto C. Tomé a , José A. S. Cavaleiro a , Fernando M. J.
Domingues a & Richard J. Cremlyn b
a Centro de Quimica do Meio Aquático (INIC), Department of
Chemistry , University of Aveiro , 3800, Aveiro, Portugal
b Division of Chemical Sciences , The University of Hertfordshire ,
Hatfield, Hertfordshire, AL10 9AB, England
Published online: 23 Sep 2006.
To cite this article: Augusto C. Tomé , José A. S. Cavaleiro , Fernando M. J. Domingues & Richard J.
Cremlyn (1993) CHLOROSULFONATION OF N-ARYLMALEIMIDES, Phosphorus, Sulfur, and Silicon and the
Related Elements, 79:1-4, 187-194, DOI: 10.1080/10426509308034412
To link to this article: http://dx.doi.org/10.1080/10426509308034412
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