Cationic cyclization of regular α-monoterpenols as a model for tri- and tetracyclic diterpene biosynthesis
作者:V.V Veselovsky、V.A Dragan、A.M Moiseenkov
DOI:10.1016/s0040-4039(00)88762-6
日期:1990.1
Low-temperature boron trifluoride etherate initiated cyclization of α-geraniol, α-nerol, and α-linalool leads to regioisomeric dimethylvinylcyclohexenes possessing a rare monoterpene carbon skeleton along with bicyclo[3.2.1]octyl fluoride. The cyclization mimics biosynthesis of tri- and tetracyclic diterpenes according to Wenkert.
低温三氟化硼醚化物引发的α-香叶醇,α-神经醇和α-芳樟醇的环化反应会导致区域异构的二甲基乙烯基环己烯具有罕见的单萜碳骨架以及双环[3.2.1]辛基氟。根据Wunkert的说法,环化模拟了三环和四环二萜的生物合成。