Inuki Shinsuke, Yoshimitsu Yuji, Oishi Shinya, Fujii Nobutaka, Ohno Hiroaki
Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan.
Org Lett. 2009 Oct 1;11(19):4478-81. doi: 10.1021/ol901904w.
Palladium(0)-catalyzed cyclization of bromoallenes bearing hydroxyl and benzamide groups as internal nucleophiles stereoselectively provides functionalized tetrahydrofuran. With this bis-cyclization as the key step, a short total synthesis of pachastrissamine, a biologically active marine natural product, was achieved.
钯(0)催化带有羟基和苯甲酰胺基团作为内部亲核试剂的溴代丙二烯的环化反应,立体选择性地生成功能化的四氢呋喃。以这种双环化反应作为关键步骤,实现了具有生物活性的海洋天然产物帕卡司他明的简洁全合成。