Article abstract of DOI:10.1080/10426509608046351

The alkenethiones, mentioned in the title, react with sodium N-chlorobenzenesulfonamides (2) to S-alkenylidene-N-arylsulfonylsulfimides (6, 9). Cyclohexenylidenesulfimides 6 are oxidized to dipolar N-(arylsulfonyl)iminioalkenesulfonamidates (7). Equilibri

Full text of DOI:10.1080/10426509608046351

This article was downloaded by: [University of Glasgow]
On: 06 January 2015, At: 20:23
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered
office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK
Phosphorus, Sulfur, and Silicon and the
Related Elements
Publication details, including instructions for authors and
subscription information:
http://www.tandfonline.com/loi/gpss20
REAKTIONEN VON THIOXOVERBINDUNGEN
MIT N-CHLORAMIDEN VII.1 5,5-
DIMETHYL-3-DIMETHYLAMINO-2-
CYCLOHEXEN-1-THION UND 3-
DIMETHYLAMINO-1-PHENYL-2-
PROPEN-1-THION MIT NATRIUM-N-
CHLORBENZOLSULFONAMIDEN
Friedrich Boberg a & Albert Otten a
a Institut für Organische Chemie der Technischen Universität
Clausthal , Leibnizstr. 6, D-38678, Clausthal-Zellefeld, Germany
Published online: 04 Oct 2006.
To cite this article: Friedrich Boberg & Albert Otten (1996) REAKTIONEN VON THIOXOVERBINDUNGEN
MIT N-CHLORAMIDEN VII.1 5,5-DIMETHYL-3-DIMETHYLAMINO-2-CYCLOHEXEN-1-THION UND 3-
DIMETHYLAMINO-1-PHENYL-2-PROPEN-1-THION MIT NATRIUM-N-CHLORBENZOLSULFONAMIDEN,
Phosphorus, Sulfur, and Silicon and the Related Elements, 112:1-4, 91-99, DOI:
10.1080/10426509608046351
To link to this article: http://dx.doi.org/10.1080/10426509608046351
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the information (the
“Content”) contained in the publications on our platform. However, Taylor & Francis,
our agents, and our licensors make no representations or warranties whatsoever as to
the accuracy, completeness, or suitability for any purpose of the Content. Any opinions
and views expressed in this publication are the opinions and views of the authors,
and are not the views of or endorsed by Taylor & Francis. The accuracy of the Content
should not be relied upon and should be independently verified with primary sources
of information. Taylor and Francis shall not be liable for any losses, actions, claims,
proceedings, demands, costs, expenses, damages, and other liabilities whatsoever or
howsoever caused arising directly or indirectly in connection with, in relation to or arising
out of the use of the Content.

This article may be used for research, teaching, and private study purposes. Any
substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing,
systematic supply, or distribution in any form to anyone is expressly forbidden. Terms &
Conditions of access and use can be found at http://www.tandfonline.com/page/terms-
and-conditions