Complete1H and13C NMR spectral assignment of 17-hydroxy epimeric sterols with planar A or A and B rings
| Autor: | Silvana Casati, Ada Manzocchi, Pierangela Ciuffreda |
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| Rok vydání: | 2004 |
| Předmět: |
Equilenin
Magnetic Resonance Spectroscopy Estradiol Stereochemistry Chemistry General Chemistry Carbon-13 NMR DEPT Boldenone Methylation Solvents medicine Proton NMR Testosterone General Materials Science Epimer Chloroform Two-dimensional nuclear magnetic resonance spectroscopy Heteronuclear single quantum coherence spectroscopy medicine.drug |
| Zdroj: | Magnetic Resonance in Chemistry. 42:360-363 |
| ISSN: | 1097-458X 0749-1581 |
| Popis: | Complete 1H and 13C spectral assignments of 17β- and 17α-hydroxy epimers of three biologically active sterols (boldenone, 3-methoxyestradiol and 3-methoxydihydroequilenin) were achieved making use of one- and two-dimensional NMR techniques (1D-HOHAHA, DEPT, COSY, NOESY, TOCSY, HSQC and COLOC). Copyright © 2004 John Wiley & Sons, Ltd. |
| Databáze: | OpenAIRE |
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