Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5307
Title: Stereoselective Synthesis of N1-6-Methyluridine and Related 2-Substituted Analogues
Authors: M., Radi
Petricci, Elena 
Corelli, Federico 
Botta, Maurizio 
Issue Date: 2007
Project: None 
Journal: HETEROCYCLES
Abstract: 
Coupling reaction of 2-substituted-6-methyl-4(3H)-pyrimidinones (la,b) with I-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose (ABR) afforded the corresponding N1-2,6-disubstituted nucleosides (2a,b) without any trace of the N3-isomer. The 2-methylthio-6-methyl derivative (2b) has then proved to be a key intermediate for the synthesis of N1-6-methyluridine (4) and the corresponding N1-2-amino-6-metyhl derivative (5), suggesting the possibility to obtain different 2,6-disubstituted derivatives by means of methylthio nucleophilic substitution. A successful solid phase application was also shown.
Description: 
36543
URI: http://hdl.handle.net/20.500.12779/5307
ISSN: 0385-5414
DOI: 10.3987/COM-06-S(K)3
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