## Abstract The total assignment of the ^1^H and ^13^C NMR spectra of five aromadendrane derivatives, (+)‐aromadendrene (1), (−)‐alloaromadendrene (2), (+)‐ledene (3), (−)‐dehydroaromadendrane (4), (−)‐globulol (5) and (+)‐viridiflorol (6) has been performed. The ^13^C spectral assignment of globul
Application of relayed coherence transfer two-dimensional nuclear magnetic resonance spectroscopy to the assignment of 1H chemical shifts in steroids
✍ Scribed by Donald W. Hughes
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 813 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Relayed coherence transfer (RELAY) two-dimensional NMR spectroscopy was demonstrated to be an effective technique for overcoming the problem of overlapping multiplets in the analysis of the 'H NMR spectra of steroids. Cross-sections through appropriate proton resonances resulted in resolved spectra of the spin systems for each of the saturated rings of the estrogenic hormones 178-and 17a-estradiol. During RELAY experiments with a fixed delay time of 0.042 s it was possible to observe RELAY cross-peaks between H-lla and 18-CH3 which resulted from magnetization transfer via long-range coupling between 1&CH3 and H-12a. The difference in stereochemistry at C-17 of these estradiol epimers allowed an examination of the effect of substituent configuration on the RELAY cross-peak intensity in order to determine the ability of the RELAY method to provide qualitative structural information.
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