Structural analysis of 25-hydroxycholesterol stereoisomers differing in configuration in position 17 and 20, by three-dimensional NMR spectra
Author:
Funder
Polish National Science Centre
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference22 articles.
1. Dependency of vicinal coupling constants on the configuration of electronegative substituents;Williams;J. Am. Chem. Soc.,1964
2. Paramagnetic shifts in solutions of cholesterol and the dipyridine adduct of trisdipivalomethanatoeuropium(III). A shift reagent;Hinkley;J. Am. Chem. Soc.,1969
3. Nuclear magnetic resonance spectroscopy. Carbon-13 spectra of steroids;Reich;J. Am. Chem. Soc.,1969
4. Steroid 13C chemical shifts. Assignments via shift reagents;Smith;J. Magn. Reson.,1973
5. 13C NMR spectra of steroids—a survey and commentary;Blunt;Org. Magn. Reson.,1977
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