share
Chin. J. Org. Chem. ›› 2007, Vol. 27 ›› Issue (9): 1126-1129. Previous Articles Next Articles
Original Articles
皮士卿a,陈新志*,a,胡四平b,潘亚金b
收稿日期:
修回日期:
发布日期:
通讯作者:
PI Shi-Qinga,CHEN Xin-Zhi*,a,HU Si-Pingb,PAN Ya-Jinb
Received:
Revised:
Published:
Contact:
Share
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
PI Shi-Qinga,CHEN Xin-Zhi*,a,HU Si-Pingb,PAN Ya-Jinb. Synthesis of Astaxanthin[J]. Chin. J. Org. Chem., 2007, 27(9): 1126-1129.
Export EndNote|Reference Manager|ProCite|BibTeX|RefWorks