作者:Stuart L. Schreiber、Conrad Santini
DOI:10.1016/s0040-4039(01)83004-5
日期:1981.1
A model study for the synthesis of the germacranes is described which utilizes a consecutive oxy-Cope/cyclobutene ring opening rearrangement sequence. The β,γ-unsaturated enone necessary for the rearrangement is obtained directly from the photocycloaddition of allene and cyclohexenone.
描述了利用连续的oxy-Cope /
环丁烯开环重排序列进行的合成ac
庚烷的模型研究。重排所必需的β,γ-不饱和烯酮直接从
丙二烯和
环己烯酮的光环加成中获得。