作者:Masahiro Yoshida、Koji Nakatani、Kozo Shishido
DOI:10.1016/j.tet.2009.05.027
日期:2009.7
The total synthesis of radulanin H and the proposed structure of radulanin E have been achieved utilizing an intramolecular condensation, sequential regioselective C- and O-allylations, and ring closing metathesis as the key steps.
radulanin H的总合成和radulanin E的拟议结构已通过分子内缩合,顺序区域选择性C和O-烯丙基化以及闭环易位作为关键步骤而实现。