Synthesis of C-Arylnucleoside Analogues
Sorbonne Universités, Université de Technologie de Compiègne, Ecole Supérieure de Chimie Organique et Minérale, Transformations Intégrées de la Matière Renouvelable, Centre de Recherche Royallieu, CS 60319, Compiègne cedex F-60203, France
Department of Chemistry, University of Hull, Hull HU6 7RX, UK
Author to whom correspondence should be addressed.
Academic Editor: Derek J. McPhee
Received: 24 January 2015 / Accepted: 10 March 2015 / Published: 18 March 2015
Modified nucleoside analogues are of great biological importance as antiviral and antitumoral agents. There is special interest in the preparation of C
-aryl nucleosides with an aromatic ring in different positions of the glycone for their biological activity. Different chemical synthesis strategies for these targets are described in this review.
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MDPI and ACS Style
Len, C.; Enderlin, G. Synthesis of C-Arylnucleoside Analogues. Molecules 2015, 20, 4967-4997.
Len C, Enderlin G. Synthesis of C-Arylnucleoside Analogues. Molecules. 2015; 20(3):4967-4997.
Len, Christophe; Enderlin, Gérald. 2015. "Synthesis of C-Arylnucleoside Analogues." Molecules 20, no. 3: 4967-4997.
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