## Abstract Extensive application of 1D and 2D NMR methodology, combined with molecular modeling, allowed the complete ^1^H and ^13^C NMR assignments of eremophilanolides from __Senecio toluccanus__. Comparison of the experimental ^1^H, ^1^H coupling constant values with those generated employing a
13C NMR assignments and conformational evaluation of diterpenes from Croton sarcopetalus Muell.
✍ Scribed by C. S. de Heluani; C. A. N. Catalán; L. R. Hernández; E. Burgueño-Tapia; P. Joseph-Nathan
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 102 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
The known diterpenes junceic acid (1) and the stress metabolite derivatives 2È4 were isolated from the hexane extracts of the roots of Croton sarcopetalus Muell. The complete 13C NMR chemical shift assignments of these compounds were achieved with the aid of DEPT and HETCOR experiments.
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