研究简报

(±)-Parvistemonine A的全合成

  • 马开庆 ,
  • 任虎斌 ,
  • 吴晓晓 ,
  • 钞建斌 ,
  • 秦雪梅
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  • a 山西大学中医药现代研究中心 太原 030006;
    b 山西大学化学化工学院 太原 030006;
    c 山西大学大型仪器中心 太原 030006

收稿日期: 2019-01-07

  修回日期: 2019-02-12

  网络出版日期: 2019-03-08

基金资助

山西省回国留学人员科研资助基金(No.2015-020)和山西省高等学校科技创新基金(No.2016115)资助项目.

Total Synthesis of Racemic (±)-Parvistemonine A

  • Ma Kaiqing ,
  • Ren Hubin ,
  • Wu Xiaoxiao ,
  • Chao Jianbin ,
  • Qin Xuemei
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  • a Modern Research Center for Traditional Chinese Medicine, Shanxi University, Taiyuan 030006;
    b College of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006;
    c Scientific Instrument Center, Shanxi University, Taiyuan 030006

Received date: 2019-01-07

  Revised date: 2019-02-12

  Online published: 2019-03-08

Supported by

Project supported by the Shanxi Scholarship Council of China (No. 2015-020) and the Science and Technology Innovation Project of Shanxi Province (No. 2016115).

摘要

Parvistemonine A为从对叶百部中分离得的百部生物碱.以化合物7为原料,通过路易斯酸催化的傅克及内酯化的串联反应,Vilsmeier-Haack及Julia-Kocienski烯烃化等6步反应首次完成了百部生物碱(±)-parvistemonine A的全合成工作,为parvistemonine A衍生物的合成和及其生物活性研究打下基础.

本文引用格式

马开庆 , 任虎斌 , 吴晓晓 , 钞建斌 , 秦雪梅 . (±)-Parvistemonine A的全合成[J]. 有机化学, 2019 , 39(7) : 2094 -2098 . DOI: 10.6023/cjoc201901010

Abstract

Parvistemonine A was isolated from Stemona parviflora. The total synthesis of racemic parvistemonine A was completed in 6 steps for the first time, employing compound 7 as the starting material. The synthetic strategy features a tandem Friedel-Crafts cyclization and lactonization, Vilsmeier-Haack and Julia-Kocienski olefination. This study laid the foundation for the synthesis of the parvistemonine A derivative and its biological activity research.

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