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
No coin nor oath required. For personal study only.
✦ 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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