Asymmetric synthesis of <i>trans-p</i>-menth-3-ene-1,2,8-triol, the monoterpene isolated from herbal plants
作者:Shunsuke Konishi、Yusuke Ogura、Hirosato Takikawa、Hidenori Watanabe
DOI:10.1080/09168451.2019.1671789
日期:2020.1.2
The monoterpene, trans-p-menth-3-ene-1,2,8-triol, is a naturally occurring alcohol isolated from several herbal plants. In the present work, the asymmetric synthesis of both enantiomers of this natural product was achieved using Sharpless asymmetric dihydroxylation as the key step. A reversal of enantiofacial selectivity was observed in the asymmetric dihydroxylation.
单萜,反式-对-薄荷脑-3-烯-1,2,8-三醇,是从数种草药植物中分离得到的天然醇。在目前的工作中,使用Sharpless不对称二羟基化作为关键步骤,实现了该天然产物的两种对映异构体的不对称合成。在不对称二羟基化反应中观察到对面选择性的逆转。