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This article has been retracted as it was submitted for publication without the prior knowledge or approval of Dr. Aloysius Siriwardena, who has contributed to the article. Additionally, it has been submitted without prior approval of the Centre National de la Recherche Scientifique (CNRS) and the laboratory in which the intellectual ideas behind the syntheses were established [1].

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  1. C. Benhaoua, “New 1,2,3-triazole iminosugars derivatives using click chemistry,” International Journal of Carbohydrate Chemistry, vol. 2012, Article ID 394574, 10 pages, 2012.
International Journal of Carbohydrate Chemistry
Volume 2012, Article ID 394574, 10 pages
Research Article

New 1,2,3-Triazole Iminosugars Derivatives Using Click Chemistry

Laboratoire Synthèse et Catalyse, LSCT, Université Ibn Khaldoun, Tiaret 14000, Algeria

Received 17 March 2012; Accepted 28 April 2012

Academic Editor: R. J. Linhardt

Copyright © 2012 Chahrazed Benhaoua. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The click concept refers ease, efficient, and the selective chemicals transformations. In this study, a novel regiospecific copper (I)-catalyzed 1, 3-dipolar of terminal alkynes to azide provided a practicable synthetic pathway of triazole iminosugars derivatives. A series of new triazole-pyrrolidinols are reported in good yield.