Complete assignment of the 1H and 13C NMR spectra of resveratrol derivatives
- 13 November 2001
- journal article
- spectral assignments-and-reference-data
- Published by Wiley in Magnetic Resonance in Chemistry
- Vol. 39 (12) , 768-770
Abstract
The complete 1H and 13C chemical shift assignments of six derivatives of resveratrol [(E)‐5‐[2‐(4‐hydroxyphenyl)ethenyl]‐1,3‐benzenediol] that possess leukotriene D4 receptor antagonistic activities are described. Two‐dimensional COSY, HMQC, HMBC and NOESY experiments, along with molecular modeling calculations, were employed to distinguish unambiguously between different configurations of the stilbene moiety. Copyright © 2001 John Wiley & Sons, Ltd.Keywords
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- Efficient Synthesis of the Carcinogenic anti-Diol Epoxide Metabolite of 5-MethylchryseneThe Journal of Organic Chemistry, 1998