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Arylamidation of Purine Nucleosides by 2-Acetylalkoxy- Aminofluorene - an Intramolecular Approach to the Synthesis of Nucleoside - Carcinogen Adducts
Authors:A Leterme  M F Lhomme  J Lhomme
Institution:Chimie Organique Biologique - UA CNRS 351 , Universite des Sciences et Techniques de Lille , Flandres - Artois, 59655, Villeneuve d'Ascq Cedex, France
Abstract:Abstract

Arylamidation of the guanosine ring at position C-8 by the carcinogen N-2acetylalkoxyaminofluorene was achieved using an intramolecular approach.
Keywords:Fluoropyrimidine  5FU  Cancer chemotherapy  Thymidylate synthase
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