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pubmed-article:11327586pubmed:abstractText1-O-Acetyl-2,3,5-tri-O-benzyl-4-thio-L-arabinofuranose (10) was transformed into the corresponding cytidine derivative 9 and the adenosine derivative 12. Both nucleosides, as well as the previously reported uridine and thymidine analogues 2 and 3, were tested for their in vitro antiviral activity.lld:pubmed
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pubmed-article:11327586pubmed:articleTitleThiosugars. Part 9: synthesis and biological evaluation of some 4'-thio-L-arabino nucleoside analogues.lld:pubmed
pubmed-article:11327586pubmed:affiliationInstitut für Organische Chemie der Universität Hamburg, Germany.lld:pubmed
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