## Abstract A complete analysis of ^1^H and ^13^C NMR spectra of the trypanocidal sesquiterpene lactone eremantholide C and two of its analogues is described. These structurally similar sesquiterpene lactones were submitted to ^1^H NMR, ^13^C {^1^H} NMR, gCOSY, gHSQC, gHMBC, **__J‐resolved__** and
✦ LIBER ✦
Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones
✍ Scribed by Daiane Cristina Sass; Vladimir Constantino Gomes Heleno; Ana Carolina Ferreira Soares; João Luis Callegari Lopes; Mauricio Gomes Constantino
- Book ID
- 113806196
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 259 KB
- Volume
- 1008
- Category
- Article
- ISSN
- 0022-2860
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