Concepedia

Investigations on sterols XI : Preparation of 13α‐androstene derivatives

Jessica Bots

Recueil des Travaux Chimiques des Pays-Bas · 1958 · 18 citations · 6 references

DOI

Concepts

Abstract

Abstract By irradiation of androst‐5‐en‐3β‐ol‐17‐one with U.V. light (λ>280mμ) 13α‐androst‐5‐en‐3β‐ol‐17‐one was obtained. This substance was converted into a mixture of the C 17 epimers of 13α‐androst‐4‐en‐17‐ol‐3‐one, both of which were obtained in a pure state.

References

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W. J. Hickinbottom · Nature · 1957 · 118 citations

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Natural products related to phenanthrene

Wm.B. Meldrum, O. T. Benfey · Journal of the Franklin Institute · 1949 · 96 citations

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William S. Johnson, D. Banerjee, William P. Schneider et al. · Journal of the American Chemical Society · 1952 · 54 citations

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Steroid Total Synthesis—Hydrochrysene Approach. VII.<sup>1</sup> Metal-in-Ammonia Reduction of the Aromatic Nucleus. dl-Epiandrosterone and the Lumi Epimer

William S. Johnson, Brian Bannister, Raphael Pappo · Journal of the American Chemical Society · 1956 · 53 citations

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Steroids. L.<sup>1</sup> The Oxidation of Steroidal Allylic Alcohols with Manganese Dioxide. A Novel Synthesis of Testosterone<sup>2</sup>

Franz Sondheimer, C. Amendolla, G. Rosenkranz · Journal of the American Chemical Society · 1953 · 53 citations

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