Preparation of ethyl 5(s),6-epoxy-3(r)-(methoxymethoxy)hexanoate: a key chiral intermediate for mevinolin and compactin.
作者:Yvan Guindon、Christiane Yoakim、Michael A. Bernstein、Howard E. Morton
DOI:10.1016/s0040-4039(00)98429-6
日期:1985.1
The synthesis of Ethyl 5(S),6-Epoxy-3(R)-(methoxymethoxy)hexanoate, a key chiral synthon for the β-hydroxy-δ-lactone portion of Mevinolin and Compactin, via a regiospecific ring opening of a tetrahydrofuran derivative by dimethylboron bromide, is described.
通过四氢呋喃的区域特异性开环合成5(S),6-Epoxy-3(R)-(甲氧基甲氧基)己酸乙酯(Mevinolin和Compactin的β-羟基-δ-内酯部分的关键手性合成子)描述了溴化二甲基硼的衍生物。