Synthesis of N-(dimethylsulfamoyl)aldimines, a new type of aldimine derivative

Article abstract of DOI:10.1080/00397919708003037

N-(Dimethylsulfamoyl)aldimines, a new type of shelf-stable aldimine derivatives, are readily prepared from aldehydes and N-(dimethylsulfamoyl)amide in refluxing toluene.

Full text of DOI:10.1080/00397919708003037

This article was downloaded by: [University of Hong Kong Libraries]
On: 21 July 2013, At: 11:18
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
Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
Publication details, including instructions for
authors and subscription information:
http://www.tandfonline.com/loi/lsyc20
Synthesis of N-
(Dimethylsulfamoyl)aldimines,
a New Type of Aldimine
Derivative
a
a
Marco Huisman , Ronald ten Have & Albert M. van
a
Leusen
a
Department of Organic and Molecular Inorganic
Chemistry, Groningen Centre for Catalysis and
Synthesis, Groningen University, Nijenborgh 4, 9747
AG, Groningen, The Netherlands
Published online: 22 Aug 2006.
To cite this article: Marco Huisman , Ronald ten Have & Albert M. van Leusen (1997)
Synthesis of N-(Dimethylsulfamoyl)aldimines, a New Type of Aldimine Derivative,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 27:6, 945-952
To link to this article: http://dx.doi.org/10.1080/00397919708003037
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