Synthesis of biheterocyclic α-aminophosphonic acid derivatives

Article abstract of DOI:10.1080/10426509808035736

We report here the synthesis of biheterocyclic a-aminophosphonic acid derivatives by 1,3 dipolar cycloaddition of acetylenic compounds, prepared in the laboratory, on α-azido α-aminophosphonic esters 1^[a].

Full text of DOI:10.1080/10426509808035736

This article was downloaded by: [University of California Santa Cruz]
On: 26 November 2014, At: 14:10
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
SYNTHESIS OF BIHETEROCYCLIC α-
AMINOPHOSPHONIC ACID DERIVATIVES
S. Achamlale a , A. Elachqar a , A. El Hallaoui a , A. Alami a , S. Elhajji a
M. L. Roumestant a c & Ph. Viallefont b
,
a Laboratoire de Chimie Organique, Faculté des Sciences Dhar El
Mehraz , Université Sidi Mohamed Ben Abdellah , Fes, Maroc
b UMR 5810, Université MONTPELLIER II , Montpellier, France
c Lab. de Chimie Org. , Université Montpellier II , 5 Av. Ch. Flahaut,
F-34060, Montpellier Cedex, France
Published online: 24 Sep 2006.
To cite this article: S. Achamlale , A. Elachqar , A. El Hallaoui , A. Alami , S. Elhajji , M. L. Roumestant &
Ph. Viallefont (1998) SYNTHESIS OF BIHETEROCYCLIC α-AMINOPHOSPHONIC ACID DERIVATIVES, Phosphorus,
Sulfur, and Silicon and the Related Elements, 140:1, 103-111, DOI: 10.1080/10426509808035736
To link to this article: http://dx.doi.org/10.1080/10426509808035736
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