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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| Veröffentlicht in: | Phytochemistry (Oxford) 1998, Vol.49 (8), p.2348-2353 |
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| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
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| Zusammenfassung: | 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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| ISSN: | 0031-9422 1873-3700 |