Komatsu H, Yamauchi S, Shimoirisa H, Ito T, Maeda M, Kojima M
Steroids. 1979 Mar;33(3):339-45. doi: 10.1016/0039-128x(79)90010-2.
6 BETA-Iodomethyl-19-norsitost-5(10)-en-3 beta-ol (V) was synthesized by homoallylic rearrangement of 19-iodositost-5-en-3 beta-ol (IV), which was obtained by the hydrolysis of 19-iodositost-5-en-3 beta-ol acetate (III) derived from the displacement of sitost-5-ene-3 beta, 19-diol 3-acetate 19-p-toluenesulfonate (I) with sodium iodide in isopropanol. The radioiodinated IV and V were prepared by isotope exchange with sodium iodide-I-131.
6β-碘甲基-19-去甲豆甾-5(10)-烯-3β-醇(V)通过19-碘豆甾-5-烯-3β-醇(IV)的高烯丙基重排反应合成,后者是由豆甾-5-烯-3β,19-二醇3-乙酸酯19-对甲苯磺酸酯(I)在异丙醇中与碘化钠发生取代反应得到的19-碘豆甾-5-烯-3β-醇乙酸酯(III)水解制得。放射性碘化的IV和V通过与碘化钠-I-131进行同位素交换来制备。