Albert Brian J, Sivaramakrishnan Ananthapadmanabhan, Naka Tadaatsu, Koide Kazunori
Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA 15260, USA.
J Am Chem Soc. 2006 Mar 8;128(9):2792-3. doi: 10.1021/ja058216u.
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.
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。