NMR study of conformation and configuration in C-20-substituted 5β,14β-pregnanes, 5β-pregn-14-enes and 21-nor-5β,14β-pregnanes
Author:
Publisher
Wiley
Subject
General Materials Science,General Chemistry
Reference18 articles.
1. A Reinvestigation of the Synthesis of 5,16-Pregnadiene-3β,20α-diol. The Nuclear Magnetic Resonance Spectra of Some Epimeric 20-Hydroxypregnane Derivatives
2. 13C NMR spectra of 5β,14β-hydroxysteroids
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1. Expedient synthesis of some novel pregnane derivatives and their evaluation as anti-oxidant and anti-dyslipidemic agents;Medicinal Chemistry Research;2009-12-24
2. Expeditious and convenient synthesis of pregnanes and its glycosides as potential anti-dyslipidemic and anti-oxidant agents;Bioorganic & Medicinal Chemistry;2007-07
3. Total assignment of1H and13C NMR spectra of pregnenolone and progesterone haptens using 2D NMR spectroscopy;Magnetic Resonance in Chemistry;1999-08
4. Synthesis and Structure−Activity Relationships of 17β-Substituted 14β-Hydroxysteroid 3-(α-l-Rhamnopyranoside)s: Steroids That Bind to the Digitalis Receptor;Journal of Medicinal Chemistry;1997-05-01
5. Structure determination of diacholestanes. Their geochemical significance;Tetrahedron;1995-02
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