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19-去甲-δ⁴-3-氧代甾体芳构化的制备化学方法。

Preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids.

作者信息

Rao P N, Cessac J W, Kim H K

机构信息

Department of Organic Chemistry, Southwest Foundation for Biomedical Research, San Antonio, Texas 78228-0147.

出版信息

Steroids. 1994 Nov;59(11):621-7. doi: 10.1016/0039-128x(94)90017-5.

Abstract

Two preparative chemical methods for aromatization of 19-nor-delta 4-3-oxosteroids are described. The first method consists of an oxidative aromatization of 19-nor-delta 4-3-oxosteroids with iodine-ceric ammonium nitrate in methanol to give a mixture of 3-methoxy ring-A aromatized derivatives consisting of the desired product, the delta 9,11 derivative, the 6-oxo derivative as well as some ring-A iodinated material. Conversion of this material to a mixture of the 3-methoxy ring-A aromatized derivative and its 6-oxo derivative was achieved by catalytic hydrogenation. Finally, reduction of the 6-oxo function with triethylsilane in trifluoroacetic acid gave the 3-methoxy-17-trifluoroacetate ring-A aromatized derivative as a single product. In the second method, reaction of 19-nor-delta 4-3-oxosteroids with copper (II) bromide in acetonitrile at room temperature resulted in aromatic steroids in a single step in excellent yields. The second method was used in the first practical chemical synthesis of a 6-dehydroestrogen from a 19-nor-delta 4,6-3-oxosteroid.

摘要

描述了两种用于19-去甲-δ⁴-3-氧代甾体芳构化的制备性化学方法。第一种方法是在甲醇中用碘-硝酸铈铵对19-去甲-δ⁴-3-氧代甾体进行氧化芳构化,得到由所需产物、δ⁹,¹¹衍生物、6-氧代衍生物以及一些A环碘化物质组成的3-甲氧基A环芳构化衍生物混合物。通过催化氢化将该物质转化为3-甲氧基A环芳构化衍生物及其6-氧代衍生物的混合物。最后,在三氟乙酸中用三乙基硅烷还原6-氧代官能团,得到单一产物3-甲氧基-17-三氟乙酸酯A环芳构化衍生物。在第二种方法中,19-去甲-δ⁴-3-氧代甾体与溴化铜(II)在乙腈中于室温下反应,一步即可得到高产率的芳香甾体。第二种方法用于首次从19-去甲-δ⁴,⁶-3-氧代甾体实际化学合成6-脱氢雌激素。

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