Selectivity in consecutive S(N)Ar-dequaternization reactions of chlorodiazines with tertiary amines

Article abstract of DOI:10.1080/00397919208019281

Consecutive S(N)Ar-dealkylation reactions of chlorodiazines such as 2-chloropyrimidine and 3,6-dichloropyridazine with tertiary amines took place in a highly selective fashion.

Full text of DOI:10.1080/00397919208019281

This article was downloaded by: [University of Cambridge]
On: 20 November 2014, At: 05:43
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
Selectivity in Consecutive SNAr-
Dequaternization Reactions of
Chlorodiazines with Tertiary
Amines
Kiyoshi Matsumoto a , Shiro Hashimoto b , Masao
Hashimoto a , Mitsuo Toda a & Sinichi Otani b
a Graduate School of Human and Environmental
Studies , Kyoto University , Kyoto, 606, Japan
b Department of Chemistry, College of Liberal Arts
and Sciences , Kyoto University , Kyoto, 606, Japan
Published online: 23 Sep 2006.
To cite this article: Kiyoshi Matsumoto , Shiro Hashimoto , Masao Hashimoto , Mitsuo
Toda & Sinichi Otani (1992) Selectivity in Consecutive SNAr-Dequaternization Reactions
of Chlorodiazines with Tertiary Amines, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 22:5, 787-792, DOI:
10.1080/00397919208019281
To link to this article: http://dx.doi.org/10.1080/00397919208019281
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