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Über Steroide und Sexualhormone. 223. Mitteilung. UV.-Bestrahlung von 11-Oxo-Steroiden I Die Darstellung von 11β, 19-Cyclo-, 9β, 19-Cyclo- und 19-Hydroxy-5α-pregnan-Verbindungen

✍ Scribed by H. Wehrli; M. S. Heller; K. Schaffner; O. Jeger


Publisher
John Wiley and Sons
Year
1961
Tongue
German
Weight
785 KB
Volume
44
Category
Article
ISSN
0018-019X

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✦ Synopsis


  1. A new two‐step process for the functionalisation of the non‐activated methyl group 19 of 5α‐steroids is described. In the first step UV.‐irradiation of the 11‐oxo‐5α‐pregnane derivate I in ethanol gives rise to a preferential attack of the photochemically excited carbonyl on methyl group 19, leading to the formation of the tertiary cyclobutanol compound II in high yield. The latter, upon treatment with lead tetraacetate in benzene solution, undergoes selective fragmentation of the photochemically formed C‐11β‐C‐19 bond furnishing the 19‐hydroxy‐11‐oxo‐5α‐ pregnane compound V.

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Über Steroide und Sexualhormone. 225. Mi
✍ M. S. Heller; H. Wehrli; K. Schaffner; O. Jeger 📂 Article 📅 1962 🏛 John Wiley and Sons 🌐 German ⚖ 962 KB

## Abstract In analogy to the previously described photochemical isomerisation of 3,20‐diethylenedioxy‐11‐oxo‐5 α‐pregnane (I → II) the UV.‐irradiation of the Δ^5^‐ and 5β‐11‐oxo‐steroids III and XXII gives rise to the 11 α‐hydroxy‐11, 19‐cyclo derivatives IV and XXIII, respectively. The observed y

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✍ Hans-Rudolf Schlatter; Christoph Lüthy; Walter Graf 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 German ⚖ 857 KB

## Abstract Starting from 19‐hydroxytestosteroneacetate (**1**) a high yield preparation of 3‐oxo‐4,4‐dimethyl‐19‐hydroxy‐5α‐steroids (__e.g.__ **7, 9, 13** and **33**) is described.