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奥生多龙的合成 被引量:2

Synthesis of Oxendolone
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摘要 以雌酚酮(Ⅱ)为原料,经8步反应合成奥生多龙(Ⅰ)。化合物Ⅴ与乙基溴化镁反应时,C16位未引入乙基,而引入了溴(Ⅺ),其结构经IR,1HNMR,MS及化学方法确证。 Oxendolone was synthesized from estrone(Ⅱ) via a eight step process. Compound(Ⅴ) reacted with ethyl magnesium bromide to give compound(Ⅺ) while the expected compound(Ⅸ) did not obtained. The structure of compound(Ⅺ) was identified by elemental analysis, IR, 1HNMR and MS.
出处 《中国药科大学学报》 CAS CSCD 北大核心 1997年第5期260-263,共4页 Journal of China Pharmaceutical University
关键词 奥生多龙 抗雄激素药物 合成 前列腺肥大 Oxendolone Anti androgenic agent Synthesis
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