研究论文

海洋天然产物呋喃二倍半萜(18S)-variabilin的全合成

  • 熊维艳 ,
  • 赵迎春 ,
  • 徐亮 ,
  • 季红
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  • a 四川大学华西药学院 天然药物系暨教育部靶向药物重点实验室 成都 610041;
    b 广州医科大学药学院 广州 511436

收稿日期: 2017-02-08

  修回日期: 2017-03-13

  网络出版日期: 2017-04-01

基金资助

国家自然科学基金(Nos.21472129,21272163)资助项目.

Total Synthesis of Marine Furanosesterterpene Natural Product, (18S)-Variabilin

  • Xiong Weiyan ,
  • Zhao Yingchun ,
  • Xu Liang ,
  • Ji Hong
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  • a Key Laboratory of Drug Targeting of Ministry of Education, and Department of Chemistry of Medicinal Natural Products, West China College of Pharmacy, Sichuan University, Chengdu 610041;
    b School of Pharmaceutical Science, Guangzhou Medical University, Guangzhou 511436

Received date: 2017-02-08

  Revised date: 2017-03-13

  Online published: 2017-04-01

Supported by

Project supported by the National Natural Science Foundation of China (Nos. 21472129, 21272163).

摘要

(18S)-variabilin是代表性的呋喃二倍半萜海洋天然产物,具有广泛的生物活性.以香叶醇为起始原料,在通过Evans不对称烷基化反应构建关键手性片段的基础上,经关键的Julia-Lythgoe偶联反应和Aldol类型缩合反应,以13步的最长线性步骤完成了(18S)-variabilin的合成.

本文引用格式

熊维艳 , 赵迎春 , 徐亮 , 季红 . 海洋天然产物呋喃二倍半萜(18S)-variabilin的全合成[J]. 有机化学, 2017 , 37(8) : 2101 -2108 . DOI: 10.6023/cjoc201702007

Abstract

(18S)-Variabilin is the representative furanosesterterpenes, which exhibits varieties of bioactivities. Starting from geraniol and the key chiral segment prepared via Evans' asymmetric alkylation protocol, (18S)-variabilin has been totally synthesized in the longest linear 13 steps involving Julia-Lythgoe coupling reaction and aldol-type condensation.

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