作者:Scott A. Snyder、Trevor C. Sherwood、Audrey G. Ross
DOI:10.1002/anie.201002264
日期:——
A polycyclic collapse: Use of a carefully designed acyclic intermediate participated in a cascade reaction that formed the entire core of the polyketide‐derived dalesconols in a single flask (see scheme). A number of additional and carefully controlled synthetic operations completed an expeditious synthesis of both of these highly bioactive natural products as well as structural congenors.
多环塌陷:使用精心设计的无环中间体参与级联反应,在单个烧瓶中形成聚酮化合物衍生的dalesconols的整个核心(见方案)。许多额外的和精心控制的合成操作完成了这些高生物活性天然产物以及结构同类物的快速合成。