Synthesis of new tri and tetraheterocyclic systems: 1,3,-Dipolar cycloaddition of nitrilimines on 2,7-dimethyl-4-phenyl-3H-1,5-benzodiazepine

Article abstract of DOI:10.1080/00397919809458689

We report here a one-step synthesis of a new series of tri and tetraheterocyclic systems by the mixed condensation reactions of N-aryl-C- ethoxycarbonylnitrilimines and diarylnitrilimines with 2,7-dimethyl-4- phenyl-3H-1,5-benzodiazepine. This 1,3-dipolar

Full text of DOI:10.1080/00397919809458689

This article was downloaded by: [Aston University]
On: 29 January 2014, At: 02:24
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 New Tri- and
Tetraheterocyclic Systems:
1,3-Dipolar Cycloaddition
of Nitrilimines on 2,7-
Dimethyl-4-Phenyl-3H-1,5-
Benzodiazepine
M. Essaber a , A. Baouid a , A. Hasnaoui a , A.
Benharref a & J.-P. Lavergne b
a Laboratoire de Chimie des Substances
Naturelles et des Hétérocycles associé au
CNCPRST, Départment de Chimie, Faculté des
Sciences-Semlalia , Université Cadi Ayyad ,
Marrakech, Maroc
b Laboratoire des Ammoacides et Peptides ,
USTL , 34095, Montpellier Cedex 5, France
Published online: 11 Mar 2009.
To cite this article: M. Essaber , A. Baouid , A. Hasnaoui , A. Benharref & J.-P.
Lavergne (1998) Synthesis of New Tri- and Tetraheterocyclic Systems: 1,3-Dipolar
Cycloaddition of Nitrilimines on 2,7-Dimethyl-4-Phenyl-3H-1,5-Benzodiazepine,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 28:22, 4097-4104, DOI: 10.1080/00397919809458689
To link to this article: http://dx.doi.org/10.1080/00397919809458689

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