Application of the study of reactivity of alkaline salts of isocyanuric acid to the synthesis of mono and trisubstituted isocyanurates

Article abstract of DOI:10.1080/00397919308013795

Reactivity of alkaline salts of isocyanuric acid has been studied. It has been established that the nucleophilic substitution is not selective because of the protonic exchanges between salts and substituted derivatives. The synthesis of mono or trisubstituted derivative is due to secondary reactions and to solvent effects. With this study, it has been possible to settle a method to prepare mono and trisubstituted derivatives of isocyanuric acid.

Full text of DOI:10.1080/00397919308013795

This article was downloaded by: [McGill University Library]
On: 29 October 2012, At: 01:47
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
Application of the Study
of Reactivity of Alkaline
Salts of Isocyanuric Acid to
the Synthesis of Mono- and
Trisubstituted Isocyanurates
Muriel Chiron-Charrier a & Paul Caubére a
a Laboratoire de Chimie Organique I, Unité associée
au CNRS n° 457, Faculté des Sciences, Université
Nancy I, B.P. 239, 54506, VANDOEUVRE LES NANCY,
FRANCE
Version of record first published: 23 Sep 2006.
To cite this article: Muriel Chiron-Charrier & Paul Caubére (1993): Application of the
Study of Reactivity of Alkaline Salts of Isocyanuric Acid to the Synthesis of Mono- and
Trisubstituted Isocyanurates, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 23:19, 2659-2672
To link to this article: http://dx.doi.org/10.1080/00397919308013795
PLEASE SCROLL DOWN FOR ARTICLE
Full terms and conditions of use: http://www.tandfonline.com/page/terms-
and-conditions

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.
The publisher does not give any warranty express or implied or make any
representation that the contents will be complete or accurate or up to
date. The accuracy of any instructions, formulae, and drug doses should be
independently verified with primary sources. The publisher shall not be liable
for any loss, actions, claims, proceedings, demand, or costs or damages
whatsoever or howsoever caused arising directly or indirectly in connection
with or arising out of the use of this material.