In addition to 1D NMR methods and 2D shift-correlated NMR techniques (COSY and HETCOR), spin-spin simulation and MMX calculations, to obtain the minimum energy conformation structure, were used for the complete 1 H and 13 C NMR assignments of stephalic acid.
Complete assignments of 1H and 13C NMR resonances of oleanolic acid, 18α-oleanolic acid, ursolic acid and their 11-oxo derivatives
✍ Scribed by Werner Seebacher; Nebojsa Simic; Robert Weis; Robert Saf; Olaf Kunert
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 86 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1214
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✦ Synopsis
Abstract
Complete assignments of ^1^H and ^13^C NMR chemical shifts for oleanolic acid, 18α‐oleanolic acid, ursolic acid and their 11‐oxo derivatives based on ^1^H, ^13^C, 2D DQF‐COSY, NOESY, HSQC, HMBC and HSQC‐TOCSY experiments were achieved. Copyright © 2003 John Wiley & Sons, Ltd.
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