Bulletin of the Korean Chemical Society

  • 제29권4호
  • /
  • Pages.847-850
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  • 2008
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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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)
  • 발행 : 2008.04.20
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초록

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.

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참고문헌

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피인용 문헌

  1. ChemInform Abstract: Synthesis of Novel Mercaptophenyl Carbocyclic C-Nucleoside Analogue (XII) Using Sequential [3,3]-Sigmatropic Rearrangement and Ring-Closing Metathesis. vol.39, pp.36, 2008, https://doi.org/10.1002/chin.200836205
  2. Modular synthesis of the pyrimidine core of the manzacidins by divergent Tsuji–Trost coupling vol.12, pp.None, 2008, https://doi.org/10.3762/bjoc.12.107