作者:Hirokazu Arimoto、Shigehiro Asano、Daisuke Uemura
DOI:10.1016/s0040-4039(99)00578-x
日期:1999.4
An asymmetric synthesis of the spirocyclic core of pinnaic acid, a cPLA2 inhibitor, is described. A key transformation in the sequence involves an asymmetric Michael-initiated ring closure.
描述了一种松果酸螺环核心(一种cPLA 2抑制剂)的不对称合成。序列中的关键转换涉及不对称的迈克尔引发的环闭合。