The hydroxylation of Δ5-androstenes by Cephalosporium aphidicola

Bensasson, Caroline M, Hanson, James R and Hunter, A Christy (1998) The hydroxylation of Δ5-androstenes by Cephalosporium aphidicola. Phytochemistry, 49 (8). pp. 2355-2358. ISSN 0031-9422

Full content URL: https://doi.org/10.1016/S0031-9422(98)00312-4

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Item Type:Article
Item Status:Live Archive

Abstract

Whereas the major hydroxylation product of 3β-hydroxy-5α-androstan-17-one by Cephalosporium aphidicola is the 11α-alcohol, the presence of a Δ5-double bond in the substrate leads to non-stereospecific allylic hydroxylation at C–7. Hydroxylation at C–11 became a minor transformation and there was no detectable hydroxylation at C–14.

Divisions:College of Science > School of Pharmacy
ID Code:45437
Deposited On:13 Jul 2021 13:05

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