Satoh A, Utamura H, Nakade T, Nishimura H
Department of Bioscience and Technology, School of Engineering, Hokkaido Tokai University, Sapporo, Japan.
Biosci Biotechnol Biochem. 1995 Jun;59(6):1139-41. doi: 10.1271/bbb.59.1139.
(+)-Eucamalol (1) and (-)-1-epi-eucamalol (2) were synthesized from (S)-(-)-perillaldehyde to determine the absolute configuration of 1, the structure of natural (+)-eucamalol being determined to be (1R,6R)-(+)-3-formyl-6-isopropyl-2-cyclohexen-1-ol. (+)-Eucamolol (1) and its 1-epimer (2) exhibited significant repellent activity against Aedes albopictus, and inhibited its feeding as well as DEET.
从(S)-(-)-紫苏醛合成了(+)-优香茅醇(1)和(-)-1-表优香茅醇(2),以确定1的绝对构型,天然(+)-优香茅醇的结构确定为(1R,6R)-(+)-3-甲酰基-6-异丙基-2-环己烯-1-醇。(+)-优香茅醇(1)及其1-差向异构体(2)对白纹伊蚊表现出显著的驱避活性,并抑制其取食,效果与避蚊胺相当。