hydroxylation of steroidal ring D lactones by Cephalosporium aphidicola

The microbiological hydroxylation of 17alpha-oxa-D-homo-5alpha-androstane-3, 17-dione, the 3beta-alcohol and the 13alpha-methyl analogue by Cephalosporium aphidicola takes place predominantly at C-7alpha in contrast to other hydroxylations by this organism.

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Published in:Phytochemistry (Oxford) 1998, Vol.49 (8), p.2348-2353
Main Authors: Hanson, J.R, Hunter, A.C
Format: Article
Language:English
Subjects:
Cephalosporium
chemical reactions
chemical structure
lactones
metabolites
steroids
transformation
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container_title Phytochemistry (Oxford)
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creator Hanson, J.R
Hunter, A.C
description The microbiological hydroxylation of 17alpha-oxa-D-homo-5alpha-androstane-3, 17-dione, the 3beta-alcohol and the 13alpha-methyl analogue by Cephalosporium aphidicola takes place predominantly at C-7alpha in contrast to other hydroxylations by this organism.
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source ScienceDirect Journals
subjects Cephalosporium
chemical reactions
chemical structure
lactones
metabolites
steroids
transformation
title hydroxylation of steroidal ring D lactones by Cephalosporium aphidicola
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