Chin. J. Org. Chem. ›› 2012, Vol. 32 ›› Issue (07): 1296-1302.DOI: 10.6023/cjoc1112152 Previous Articles     Next Articles

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柚皮苷半合成生物活性黄酮醇和橙酮类化合物研究

吴峥, 蔡双莲, 范文金, 汪秋安   

  1. 湖南大学化学化工学院 长沙 410082
  • 收稿日期:2011-12-15 修回日期:2012-02-21 发布日期:2012-03-08
  • 通讯作者: 汪秋安 E-mail:wangQA@hnu.edu.cn
  • 基金资助:
    湖南省研究生科研创新项目(2010 年)和湖南省科技计划(No. 2011FJ3214)资助项目.

Semisynthesis of Bioactive Flavonols and Aurones from Naringin

Wu Zheng, Cai Shuanglian, Fan Wenjin, Wang Qiuan   

  1. College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082
  • Received:2011-12-15 Revised:2012-02-21 Published:2012-03-08
  • Supported by:
    Project supported by the Hunan Provinical Innovation Foundation for Postgraduate (2010) and the Hunan Provincal Science & Technology Plan (No. 2011FJ3214).

Four natural flavonols kaemferol (1), 3-hydroxy-5, 7, 4′-trimethoxy flavone (2) 3, 5-dihydroxy-7, 4′-dimethoxy flavone (3), rhamnocitrin (4) and two novel aurones 4, 6, 4′-trihydroxydihydroaurone (5), 4-hydroxy-6, 4′-dimethoxy dihydroaurone (6) were semi synthesized by reaction steps including glycoside hydrolysis, dehydrogenation, benzyl protection, O-methylation, DMDO oxidation or Algar-Flynn-Oyamade (AFO) reaction and debenzylation. The synthetic methods of DMDO oxidation for flavones to flavonols and AFO reaction for chalcones to aurones were efficient improved in the key steps. The structures of all synthetic compounds have been confirmed by NMR, MS and IR spectra. The synthetic methods have the advantages of easy availability of starting materials, simple operation and good yields, so it has considerable practical value.

Key words: Naringin, Flavonols, Aurones, dimethyldioxirane (DMDO) oxidation, semisynthesis