Microbial hydroxylation of epiandrosterone by Aspergillus candidus
Author:
Affiliation:
1. Department of Chemistry, Faculty of Arts and Sciences, Sakarya University, Sakarya, Turkey
Publisher
Informa UK Limited
Subject
Biochemistry,Catalysis,Biotechnology
Link
https://www.tandfonline.com/doi/pdf/10.1080/10242422.2017.1289184
Reference35 articles.
1. Microbiological hydroxylation of steroids. Part VI. Hydroxylation of simple mono- and di-oxygenated 5α-androstanes and of 3-oxoestranes with the fungus Aspergillus ochraceus
2. Microbiological hydroxylation of steroids. Part IX. Hydroxylation of diketones and keto-alcohols derived from 5α-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signals
3. Microbiological hydroxylation of steroids. Part XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5α-androstanes and to 5α-androstan-11-one
4. Microbiological hydroxylation. Part XVIII. Introduction of 16α-, 9α-, and 3α-hydroxy-groups into dioxygenated 5α-androstanes by the fungus Diaporthe celastrina
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