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Synthesis of 9-[2′,3′-dideoxy-2′,3′-bis-C-hydroxymethyl-α-l-threofuranosyl]adenine and its 4′-thio analog as potential antiviral agents

✍ Scribed by Yoshiko Kikuchi; Hiroko Kurata; Shigeru Nishiyama; Shosuke Yamamura; Kuniki Kato


Book ID
104257392
Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
217 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


The enantiomerically pure synthesis of 9-[2',3'-dideoxy-2',3'-bis-C-hydroxymethyl-c~-Lthreofuranosyl]adenine and its 4'-thio analog was achieved via coupling of silylated 6-chloropurine with l-O-acetylfuranose derivative 17 and its 4'-thio analog 24, respectively, prepared from (+)-diethyl Ltartrate.


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ChemInform Abstract: Synthesis of 4-Subs
✍ Johanna Wachtmeister; Anna Muehlman; Bjoern Classon; Bertil Samuelsson 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

## Synthesis of 4-Substituted Carbocyclic 2,3-Dideoxy-3-Chydroxymethyl Nucleoside Analogues as Potential Antiviral Agents. -Evaluation of the title compounds for their anti-HIV-1 activity and cytopathic effects reveals that they are inactive. -(WACHTMEISTER,