作者:M. Metzler
DOI:10.1016/0040-4020(78)87007-0
日期:1978.1
and some of its derivatives have been synthesized from α-dienestroldiacelate via the ω-bromo- and ω-acetoxy-β-dienestroldiacetate. The NMR and mass spectra of these compounds and their stereochemistry are discussed. Thin layer chromatography, gas chromatography and mass spectrometry show that synthetic ω-hydroxy-β-dienestrol is identical with a major metabolite of diethylstilbestrol. The identity is
ω-羟基-β-二烯雌酚及其一些衍生物是通过ω-溴-和ω-乙酰氧基-β-二烯雌酚二乙酸酯由α-二烯雌醇二酯合成的。讨论了这些化合物的NMR和质谱图及其立体化学。薄层色谱,气相色谱和质谱分析表明,合成的ω-羟基-β-二烯雌酚与己烯雌酚的主要代谢物相同。通过乙酰化代谢物的反向同位素稀释分析进一步证实了该特性。在4-(对硝基苄基)吡啶试验中显示出ω-乙酰氧基-β-二烯雌酚二乙酸酯具有烷基化潜力。