趙剛
摘要:采用仿生生源合成策略,金粟蘭內酯(+)-chloranthalactone F被首次合成。探索了如何構建(+)-chloranthalactone F 的生源前體3/5/6三環不飽和內酯(+)-chloranthalactone A。從(R)-Hajos-Wiechert酮出發,選擇性合成了熱力學不穩定的反式氫化茚酮,經Wharton 轉化和 Simmons-Smith環丙烷化等關鍵步驟,制備了3/5/6三環不飽和內酯(+)-chloranthalactone A,最終經[2+2]仿生途經完成了首次(+)-chloranthalactone F全合成。該工作揭示了(+)-chloranthalactone F的生源合成途徑以及確定其絕對構型。
關鍵詞:全合成;倍半萜;chloranthalactone A; chloranthalactone F
Total synthesis of sesquiterpenoid chloranthalactone A and F
Abstract:Total synthesis of (+)-chloranthalactone F was first been accomplished via biomimetic synthetic strategies. Firstly, the synthetic strategies to the unsaturated lactones and the construction of the 3/5/6 tricyclic framework were probed into the biomimetic monomer named (+)-chloranthalactone A. Starting from the prepared (R)-Hajos-Wiechert ketone, a trans-fused, thermodynamically unstable hydrindanone was synthesized and further exploration ensured the asymmetric synthesis of congested 3/5/6 core skeleton by way of Wharton transposition and Simmons-Smith reaction. Subsequently, the syntheses of unsaturated lactones were accomplished basing on the strategies of ketone transposition and [2+2] electro-cyclization/ring-opening/lactonization. This work has revealed biogenesis pathway of (+)-chloranthalactone F and to determine its absolute configuration.
Keywords:Total synthesis; sesquiterpenoid; chloranthalactone A; chloranthalactone F
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