Photochemische Reaktionen. 24. Mitteilung. Die UV.‐Bestrahlung von Testosteron und 3‐Oxo‐17β‐acetoxy‐Δ 1;5 ‐androstadien. (Vorläufige Mitteilung) | Zendy

Nann B. | Zendy; Gravel D. | Zendy; Schorta R. | Zendy; Wehrli H. | Zendy; Schaffner K. | Zendy; Jeger O. | Zendy

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Photochemische Reaktionen. 24. Mitteilung. Die UV.‐Bestrahlung von Testosteron und 3‐Oxo‐17β‐acetoxy‐Δ 1;5 ‐androstadien. (Vorläufige Mitteilung)

Author(s) -

Nann B.,

Gravel D.,

Schorta R.,

Wehrli H.,

Schaffner K.,

Jeger O.

Publication year - 1963

Publication title -

helvetica chimica acta

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.74

H-Index - 82

eISSN - 1522-2675

pISSN - 0018-019X

DOI - 10.1002/hlca.19630460702

Subject(s) - chemistry , stereospecificity , solvent , reactivity (psychology) , steroid , medicinal chemistry , photochemistry , stereochemistry , organic chemistry , hormone , catalysis , biochemistry , medicine , alternative medicine , pathology

1. The photochemical reactivity of testosterone ( 1 ) is strongly influenced by the nature of the solvent. Dimerization (→ 18 ), pinacone formation (→ 19 )), reactions between the steroid and the solvent molecules (→ 20a , 20b , 21 ) and stereospecific isomerizations (→ 2 , 4 ) are observed.

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