作者:Susumu Ohira、Naoya Yoshihara、Taisuke Hasegawa
DOI:10.1246/cl.1998.739
日期:1998.8
A spiro sesquiterpene alcohol, (−)-gleenol (1) was synthesized from (−)-l-menthol in 16 steps, using the C-H insertion reaction of the alkylidenecarbene as the key step. The absolute configuration of (−)-1 was determined to be 1S, 6R, 7S, 10R.
以亚烷基卡宾的 CH 插入反应为关键步骤,由 (-)-l-薄荷醇分 16 步合成螺倍半萜醇 (-)-gleenol (1)。(-)-1 的绝对构型确定为 1S、6R、7S、10R。