Total synthesis of FR901464, an antitumor agent that regulates the transcription of oncogenes and tumor suppressor genes

被引:76
作者
Albert, BJ [1 ]
Sivaramakrishnan, A [1 ]
Naka, T [1 ]
Koide, K [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
关键词
D O I
10.1021/ja058216u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
FR901464 is a potent anticancer agent that regulates the transcription of oncogenes and tumor suppressor genes. A convergent enantioselective synthesis of FR901464 was accomplished in 13 linear steps. Central to the synthetic approach was the diene-ene cross olefin metathesis reaction to generate the C6-C7 olefin, without the use of protecting groups, as the final coupling. Additional key reactions include a Zr/Ag-promoted alkynylation to set the C4 stereocenter, a mild and chemoselective Red-Al reduction, a stereoselective Mislow-Evans-type [2,3]-sigmatropic rearrangement to install the C5 stereocenter, a Carreira asymmetric alkynylation to generate the C4′ stereocenter, and a highly efficient ring-closing metathesis-allylic oxidation sequence to form an unsaturated lactone. Copyright © 2006 American Chemical Society.
引用
收藏
页码:2792 / 2793
页数:2
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