作者:Nalin B. Das、Kurt B.G. Torssell
DOI:10.1016/s0040-4020(01)91943-x
日期:——
The target molecule 1b has been prepared by a new methodology via silyl nitronates and 2-isoxazolines. Since 1a was converted earlier into PGE1 our approach constitutes a novel entrance to prostaglandins.
目标分子1b已经通过新的方法经由甲硅烷基磺酸盐和2-异恶唑啉制备。由于1a较早地转换为PGE 1,因此我们的方法构成了前列腺素的新颖入口。