[将3-酮-19-去甲-5(10)-烯甾体微生物还原为相应的3-羟基化合物] - Suppr | 超能文献

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[Microbiological reduction of 3-keto-19-nor-5(10)-ene steroids to the corresponding 3-hydroxy-compounds].[将3-酮-19-去甲-5(10)-烯甾体微生物还原为相应的3-羟基化合物]

Chem Ber. 1970;103(2):603-9. doi: 10.1002/cber.19701030232.

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[Microbiological transformation of 3-alkoxy-19-nor-2.5(10)-diene steroids to 3-hydroxy-5(10)-ene structures].[3-烷氧基-19-降-2,5(10)-二烯甾体向3-羟基-5(10)-烯结构的微生物转化]

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Aromatization of 9alpha-hydroxy-19-norandrostenedione by Arthrobacter simplex.简单节杆菌对9α-羟基-19-去甲雄烯二酮的芳构化作用

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4

Microbiological hydroxylation of steroids. VI. Hydroxylation of simple mono- and di-oxygenated 5 -androstanes and of 3-oxoestranes with the fungus Aspergillus ochraceus.

J Chem Soc Perkin 1. 1972;23:2930-6. doi: 10.1039/p19720002930.

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Microbiological hydroxylation of steroids. 3. A convenient, microbiological route to 15-oxygenated 5-alpha-androstanes.

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Metabolism of unsaturated bile acids and androstanes by human faecal bacteria.人粪便细菌对不饱和胆汁酸和雄烷类的代谢

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7

Microbiological transformation of steroids. I. The synthesis of 19-nortestololactone.

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Microbial hydroxylations. II. Oxidative cleavage of the 17-beta-acetyl side-chain of progesterone by Aspergillus ochraceus.

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Microbiological hydroxylation. Part XVI. Incubation of derivatives (mainly acetals) of 5alpha-androstane ketones with the fungi Calonectria decora, Aspergillus ochraceus, and Rhizopus nigricans.微生物羟基化作用。第十六部分。5α-雄甾烷酮的衍生物（主要是缩醛）与真菌德氏弯孢霉、赭曲霉和黑根霉的培养。

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Microbiological hydroxylation of steroids. XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5 alpha-androstanes and to 5 alpha-androstan-11-one.甾体的微生物羟基化作用。XI. 合成3,7-、3,11-、3,12-、7,11-、7,17-和11,17-双氧化5α-雄甾烷以及5α-雄甾-11-酮的简便方法。

J Chem Soc Perkin 1. 1974;2:312-7. doi: 10.1039/p19740000312.