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首页> 外文期刊>Russian Journal of Organic Chemistry >Synthesis of 17alpha-Acetoxyestra-1,3,5(10)-triene-3,11alpha-diol
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Synthesis of 17alpha-Acetoxyestra-1,3,5(10)-triene-3,11alpha-diol

机译:17α-乙酰氧基-1,3,5(10)-三烯-3,11α-二醇的合成

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摘要

Introduction of a hydroxy group into position 11 of natural estrogens and its subsequent modification often enhance biological activity of the initial steroid and endows it with new properties [1-3].11alpha-Hydroxy-estra-1,3,5(10)-trienes can also be used as synthons for the preparation of various 19-norsteroids [4];for example,compounds exhibiting antitumor activity were obtained on the basis of such 17alpha-ethynylestradiol analogs [5].
机译:将羟基引入天然雌激素的11位及其后续修饰通常会增强初始类固醇的生物活性,并赋予其新的特性[1-3] .11alpha-Hydroxy-estra-1,3,5(10)-三烯也可以用作合成子来制备各种19-降甾类化合物[4];例如,在此类17α-乙炔基雌二醇类似物的基础上获得了具有抗肿瘤活性的化合物[5]。

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