Issue 22, 1989
From the journal:

Journal of the Chemical Society, Chemical Communications

Stereochemistry of reduction by the 5α-reductase enzyme of Penicillium decumbens and the 1H NMR assignment of 5α-dihydrotestosterone

Herbert L. Holland,   Weili Xu  and  Donald W. Hughes  

Abstract

Reduction of the alkenic bond of testosterone and androst-4-ene-3,17-dione by the 5α-reductase enzyme of Penicillium decumbens proceeds with trans stereochemistry.

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Article information

DOI
https://doi.org/10.1039/C39890001760
Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1760-1761

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Stereochemistry of reduction by the 5α-reductase enzyme of Penicillium decumbens and the 1H NMR assignment of 5α-dihydrotestosterone

H. L. Holland, W. Xu and D. W. Hughes, J. Chem. Soc., Chem. Commun., 1989, 1760 DOI: 10.1039/C39890001760

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