Carbon-13 nuclear magnetic resonance spectra of bile acid derivatives. Part II. Mono-, di- and trihydroxy stereoisomers of methyl 5α-cholanoates
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Organic Chemistry,Molecular Biology,Biochemistry
Reference22 articles.
1. Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
2. 13C n.m.r. spectra of steroids —a survey and commentary
3. Nuclear magnetic resonance spectroscopy. Carbon-13 spectra of cholic acids and hydrocarbons included in sodium desoxycholate solutions
4. Differentiation between the 25R- and 25S-isomers of 5 beta-cholestane-3 alpha, 7 alpha, 26-triol by 13C NMR spectroscopy.
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1. Novel, major 2α- and 2β-hydroxy bile alcohols and bile acids in the bile of Arapaima gigas, a large South American river fish;Steroids;2016-03
2. Chemical synthesis of the (25R)- and (25S)-epimers of 3α,7α,12α-trihydroxy-5α-cholestan-27-oic acid as well as their corresponding glycine and taurine conjugates;Chemistry and Physics of Lipids;2011-07
3. Bioproduction of bile acids and the glycine conjugates by Penicillium fungus;Journal of Natural Medicines;2007-08-21
4. Bile Acids as Building Blocks of Supramolecular Hosts;Molecules;2001-01-16
5. Potential bile acid metabolites. 20. A new synthetic route to stereoisomeric 3,6,-dihydroxy- and 6-hydroxy-5α-cholanoic acids;Steroids;1993-08
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