Zhong Li-Ping, Gudeman Cyrus, Zhen Jingsong, Wanasinghe Oshani A, Hellmig Jacob, Collins Michael J E, Bacsa John, Adibekian Alexander, Dai Mingji
Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
Department of Chemistry, University of Illinois Chicago, Chicago, Illinois 60607, United States.
J Am Chem Soc. 2025 Aug 13;147(32):28589-28594. doi: 10.1021/jacs.5c08224. Epub 2025 Aug 4.
We report an asymmetric total synthesis of (-)-neocucurbol C, a diterpene natural product possessing a unique and complex 6/6/5/5/6 polycyclic skeleton and nine stereocenters. Pattern-recognition analysis led us to the chiral pool molecule (+)-nootkatone as the starting material, already containing the AB ring system and two key stereocenters encoded by the target molecule. The extra isopropenyl group of (+)-nootkatone was removed by Kwon's hydrodealkenylative bond fragmentation. Other key steps include a Suzuki-Miyaura cross coupling to introduce an aromatic ring as the E ring precursor, an oxidative dearomatization cyclization to form the key oxa-bridge, and a metal-catalyzed hydrogen atom transfer (MHAT)-initiated reductive radical cyclization to complete the entire framework for subsequent peripheral decorations, which eventually delivered (-)-neocucurbol C in 24 steps for the first time. In addition, the cytotoxicity evaluation of (-)-neocucurbol C and its synthetic intermediates against multiple cancer cell lines identified new lead compounds with promising anticancer activity for further development.
我们报道了(-)-新葫芦素C的不对称全合成,这是一种二萜类天然产物,具有独特而复杂的6/6/5/5/6多环骨架和九个立体中心。模式识别分析使我们选择手性源分子(+)-诺卡酮作为起始原料,它已经包含AB环系统和目标分子编码的两个关键立体中心。(+)-诺卡酮的额外异丙烯基通过权氏加氢脱烯基键断裂反应去除。其他关键步骤包括通过铃木-宫浦交叉偶联反应引入一个芳香环作为E环前体,氧化去芳构化环化反应形成关键的氧桥,以及金属催化的氢原子转移(MHAT)引发的还原自由基环化反应以完成整个骨架以便后续进行外围修饰,最终首次通过24步反应得到了(-)-新葫芦素C。此外,对(-)-新葫芦素C及其合成中间体针对多种癌细胞系的细胞毒性评估鉴定出了具有有望的抗癌活性的新先导化合物,以供进一步开发。