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http://dx.doi.org/10.5012/bkcs.2008.29.4.847

Synthesis of Novel Mercaptophenyl Carbocyclic C-Nucleoside Analogue Using Sequential [3,3]-Sigmatropic Rearrangement and Ring-closing Metathesis  

Li, Hua (BK-21 Project Team, College of Pharmacy, Chosun University)
Hong, Joon-Hee (BK-21 Project Team, College of Pharmacy, Chosun University)
Publication Information
Bulletin of the Korean Chemical Society / v.29, no.4, 2008 , pp. 847-850 More about this Journal
Abstract
Novel mercaptophenyl carbocyclic C-nucleoside analogue was synthesized via a cyclopentenol intermediate 10, which was prepared using a sequential [3,3]-sigmatropic rearrangement and ring-closing metathesis (RCM). Friedel-Crafts alkylation was then used to couple the thiophenol.
Keywords
Carbocyclic C-nucleoside; [3,3]-Sigmatropic rearrangement; Ring-closing metathesis; Friedel-Crafts alkylation
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