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FR901464的全合成,一种调节癌基因和肿瘤抑制基因转录的抗肿瘤药物。

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

作者信息

Albert Brian J, Sivaramakrishnan Ananthapadmanabhan, Naka Tadaatsu, Koide Kazunori

机构信息

Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA 15260, USA.

出版信息

J Am Chem Soc. 2006 Mar 8;128(9):2792-3. doi: 10.1021/ja058216u.

Abstract

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.

摘要

FR901464是一种有效的抗癌剂,可调节癌基因和肿瘤抑制基因的转录。通过13步线性反应完成了FR901464的对映选择性汇聚合成。该合成方法的核心是二烯-烯交叉烯烃复分解反应,用于生成C6-C7烯烃,且无需使用保护基团作为最终偶联反应。其他关键反应包括锆/银促进的炔基化反应以确定C4立体中心、温和且具有化学选择性的Red-Al还原反应、用于构建C5立体中心的立体选择性米斯洛-埃文斯型[2,3]-σ迁移重排反应、用于生成C4'立体中心的卡雷拉不对称炔基化反应,以及用于形成不饱和内酯的高效闭环复分解-烯丙基氧化序列。

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