Stereochemistry in dehydrogenation of 3α, 7α, 12α-trihydroxy-5β-cholestan-26-oyl CoA during cholic acid biosynthesis
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940002325
Reference12 articles.
1. L. Stryer , Biochemistry, W. H. Freeman & Co., New York, 3rd edn., 1988, p. 467.
2. Non-stereoselective Formation of 3.ALPHA.,7.ALPHA.,12.ALPHA.,24-Tetrahydroxy-5.BETA.-cholestan- 26-oic Acid during Cholic Acid Biosynthesis.
3. Non-stereoselective conversion of the four diastereoisomers at the C-24 and C-25 positions of 3.ALPHA.,7.ALPHA.,12.ALPHA.,24-tetrahydroxy-5.BETA.-cholestan-26-oic acid into cholic acid.
4. Study on Stereospecificity of Enzyme Reaction Related to Peroxisomal Bile Acid Synthesis in Rat Liver.
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1. Steroids: reactions and partial synthesis;Natural Product Reports;1996
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