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首页> 外文期刊>Chemistry of heterocyclic compounds >Synthesis and molecular structure study of 3-methoxy-7α-methyl-6-oxa- 9β,14β-estra-1,3,5(10)-trien-17-one in solution
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Synthesis and molecular structure study of 3-methoxy-7α-methyl-6-oxa- 9β,14β-estra-1,3,5(10)-trien-17-one in solution

机译:溶液中3-甲氧基-7α-甲基-6-氧杂-9β,14β-estra-1,3,5(10)-trien-17-one的合成及分子结构研究

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摘要

It was established by NMR spectroscopy that the catalytic hydrogenation of 3-methoxy-7α-methyl-6-oxa-14β-estra-1,3,5(10),8-tetraen-17-one leads to the formation of 3-methoxy-7α-methyl-6-oxa-9β,14β-estra-1,3, 5(10)-trien-17-one, the structure of which was investigated in solution. The corresponding analog with a free hydroxyl group at the position 3 possesses an antiradical activity at the absence of uterotropic effect.
机译:通过NMR光谱法确定3-甲氧基-7α-甲基-6-氧杂-14β-estra-1,3,5(10),8-丁烯-17-的催化氢化导致3-的形成甲氧基-7α-甲基-6-氧杂-9β,14β-雌激素-1,3,5(10)-三烯-17-一,在溶液中研究了其结构。相应的在3位具有游离羟基的类似物在不存在促同尿作用的情况下具有抗自由基活性。

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