作者:Ae. de Groot、M.P. Broekhuysen、L.L. Doddema、M.C. Vollering、J.M.M. Westerbeek
DOI:10.1016/s0040-4039(00)85725-1
日期:1982.1
a sesquiterpene with a rearranged drimane skieleton, is described using 6β, 8aβ-dimethyl-5-methylene-3,4,4aα, 5,6,7,8,8a-octahydro-1(2H)-naphtalenone (10) as a key intermediate. A new annelation method for butenolides via hydrolysis of a thiohenyl furan is reported.
使用6β,8aβ-二甲基-5-亚甲基-3,4,4aα,5描述了(±)-色氨酸4(13),8-二烯内酯(1),一种具有重排的drimane骨架的倍半萜的全合成。 ,6,7,8,8a-八氢-1(2H)-萘烯酮(10)作为关键中间体。报道了一种通过苯硫基呋喃水解水解丁烯内酯的新的去核方法。