Chin. J. Org. Chem. ›› 2007, Vol. 27 ›› Issue (9): 1126-1129. Previous Articles     Next Articles

Original Articles

虾青素的合成

皮士卿a,陈新志*,a,胡四平b,潘亚金b   

  1. (a浙江大学材料与化工学院 杭州 310027)
    (b浙江医药股份有限公司新昌制药厂 新昌 312500)
  • 收稿日期:2006-02-14 修回日期:2006-11-02 发布日期:2007-08-30
  • 通讯作者: 陈新志

Synthesis of Astaxanthin

PI Shi-Qinga,CHEN Xin-Zhi*,a,HU Si-Pingb,PAN Ya-Jinb   

  1. (a College of Materials Science and Chemical Engineering, Zhejiang University, Hangzhou 310027)
    (b Xinchang Pharmaceuticals Factory, Zhejiang Medicine Co., LTD., Xinchang 312500)
  • Received:2006-02-14 Revised:2006-11-02 Published:2007-08-30
  • Contact: CHEN Xin-Zhi

Astaxanthin was synthesized from α-ionone via the route of 2C15+C10→C40. In which the key intermediate of C15 building block, 6-hydroxy-3-(3-hydroxy-3-methyl-1,4-pentadien-1-yl)-2,4,4-trimethyl- 2-cyclohexen-1-one was obtained by selectively epoxidizing the double bond of trimethylsilyl enol ether as a key step.

Key words: α-ionone, astaxanthin, carotenoid, 2,7-dimethyl-2,4,6-octantrien-1,8-dial, 6-hydroxy-3-(3-hydroxy-3-methyl-1,4-pentadien-1-yl)- 2,4,4-trimethyl-2-cyclohexen-1-one