作者:Shunsaku Ohta、Naoki Tsuno、Kazushi Maeda、Seikou Nakamura、Norio Taguchi、Masayuki Yamashita、Ikuo Kawasaki
DOI:10.1016/s0040-4039(00)00678-x
日期:2000.6
The first total synthesis of clathridine A (8), a marine imidazole alkaloid, was achieved by using a novel regioselective condensation as a key step, in which preclathridine A (2) was treated with 1-methylparabanic acid (11) in the presence of a silylating agent.
clathridine A的第一全合成(8),海洋咪唑生物碱,通过使用一种新颖的区域选择性缩合作为关键步骤,其中preclathridine A(达到2)与1- methylparabanic酸(处理过的11)中的存在甲硅烷基化剂。