Bell T W, Boppré M, Schneider D, Meinwald J
Experientia. 1984 Jul 15;40(7):713-4. doi: 10.1007/BF01949738.
The biosynthetic conversion of a pyrrolizidine alkaloid (heliotrine, IV) to a male moth pheromone (hydroxydanaidal, III) is found to proceed with inversion of configuration at the remaining asymmetric center (C-7).
已发现吡咯里西啶生物碱(天芥菜碱,IV)生物合成转化为雄蛾性信息素(羟基达纳醛,III)时,在剩余的不对称中心(C-7)发生构型翻转。