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Asymmetric synthesis of enantiomerically pure (−)-(1′R,4′R)-dioxolane-thymine and its anti-HIV activity.

✍ Scribed by Chung K. Chu; Soon K. Ahn; H.O. Kim; J.Warren Beach; Antonio J. Alves; Lak S. Jeong; Qamrul Islam; Patrick Van Roey; Raymond F. Schinazi


Book ID
104215965
Publisher
Elsevier Science
Year
1991
Tongue
French
Weight
277 KB
Volume
32
Category
Article
ISSN
0040-4039

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✦ Synopsis


An asymmetric synthesis leading to the enannomerically pwe dioxolane-T hm been achieved and its crystal structure has been demmined and compared to the previousty reported racemate. (-)-(I 'R,I'R)-L%xolane-T war found to have potent and selective anti-HIV activity

in primary human lymphocytes.


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Asymmetric Synthesis via Acetal Template
✍ R.G. Andrew; R.E. Conrow; J.D. Elliott; W.S. Johnson; S. Ramezani 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 240 KB

## Several (3S,4S)-and (3S,4R)-statine derivatives have been prepared by attack of nucleophiles on crystalline, epimeric N-BOC-lactams 7a and 76. The key step in the synthesis of the lactams was the TiC/4-catalyzed coupling reactions of acetals derived from (R)-1,3-butanediol with a//y/trimethy/si