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(+)-哈帕啡 G 的全合成。

Total Synthesis of (+)-Haperforin G.

机构信息

Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education and Beijing National Laboratory for Molecular Science (BNLMS), and Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.

Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Shenzhen 518055, China.

出版信息

J Am Chem Soc. 2020 Nov 18;142(46):19487-19492. doi: 10.1021/jacs.0c10122. Epub 2020 Nov 5.

Abstract

A concise chemical synthesis of (+)-haperforin G in 20 steps from commercially available starting materials is achieved with the integration of the Co-catalyzed intramolecular Pauson-Khand reaction for the stereoselective construction of cyclopentanone bearing an all-carbon quaternary stereogenic center at the bridge-head position and the light-initiated photocatalysis for convergent and asymmetric cross-coupling of the unstabilized C(sp)-radical with an enone. The developed chemistry paves the way to synthesizing structurally diverse analogs of haperforin G ().

摘要

从商业可得的起始原料出发,经 20 步反应即可实现(+)-海鞘素 G 的简洁化学全合成,该过程通过协同催化的分子内环 Pauson-Khand 反应实现了桥环位连有全碳季碳中心的环戊酮的立体选择性构建,并结合光引发的光催化反应实现了未稳定 C(sp3)-自由基与烯酮的对映体富集的交叉偶联。所开发的化学合成路线为合成结构多样的海鞘素 G 类似物()奠定了基础。

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