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
-
Published:1974
Issue:0
Volume:
Page:312-317
-
ISSN:0300-922X
-
Container-title:J. Chem. Soc., Perkin Trans. 1
-
language:en
-
Short-container-title:J. Chem. Soc., Perkin Trans. 1
Author:
Bell Alan M.,Chambers Virginia E. M.,Ewart Sir,Jones R. H.,Meakins G. Denis,Müller Wilhelm E.,Pragnell John
Publisher
Royal Society of Chemistry (RSC)
Cited by
15 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Silver(I) Carbonate on Celite;Encyclopedia of Reagents for Organic Synthesis;2017-04-12
2. Microbial hydroxylation of epiandrosterone by Aspergillus candidus;Biocatalysis and Biotransformation;2017-02-26
3. Catalytic Oxidations of Steroid Substrates by Artificial Cytochrome P-450 Enzymes;The Journal of Organic Chemistry;2002-06-06
4. Silver(I) Carbonate on Celite;Encyclopedia of Reagents for Organic Synthesis;2001-04-15
5. Oxidation Reactions;Biotransformations in Preparative Organic Chemistry;1989