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Nucleosides and Nucleotides Volume 6, 1987 - Issue 1-2
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Arylamidation of Purine Nucleosides by 2-Acetylalkoxy- Aminofluorene - an Intramolecular Approach to the Synthesis of Nucleoside - Carcinogen Adducts

A. Leterme Chimie Organique Biologique - UA CNRS 351, Universite des Sciences et Techniques de Lille, Flandres - Artois, 59655, Villeneuve d'Ascq Cedex, France
,
M. F. Lhomme Chimie Organique Biologique - UA CNRS 351, Universite des Sciences et Techniques de Lille, Flandres - Artois, 59655, Villeneuve d'Ascq Cedex, France
&
J. Lhomme Chimie Organique Biologique - UA CNRS 351, Universite des Sciences et Techniques de Lille, Flandres - Artois, 59655, Villeneuve d'Ascq Cedex, France
Pages 401-402 | Published online: 05 Dec 2006
 
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Abstract

Arylamidation of the guanosine ring at position C-8 by the carcinogen N-2acetylalkoxyaminofluorene was achieved using an intramolecular approach.

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