## Abstract In this work we describe the complete ^1^H and ^13^C NMR analyses of three arylnaphtalene lignan lactones (taiwanin C, 4‐methyl dehydroretrodendrin and justicidin B) using modern NMR techniques such as gCOSY, nonedited gHSQC, gHMBC and NOE experiments. Complete assignment and homonuclea
Complete assignments of 1H and 13C NMR spectral data for benzylidenebenzyl butyrolactone lignans
✍ Scribed by Rosangela da Silva; Susimaire Pedersoli; Valdemar Lacerda Junior; Paulo Marcos Donate; Sérgio de Albuquerque; Jairo Kenupp Bastos; Ana Lúcia Santos de Matos Araújo; Márcio Luis Andrade e Silva
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 94 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1655
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✦ Synopsis
Abstract
The structures of three benzylidenebenzyl butyrolactone lignans (gossypifan, carthamogenin, and savinin) have been established on basis of ^1^H NMR and ^13^C NMR spectroscopic data. The ^1^H NMR and ^13^C NMR spectra of these lignans have been fully assigned by the use of techniques such as gCOSY, non‐edited gHSQC, and gHMBC. Complete assignment and most homonuclear hydrogen coupling constant measurements were performed, also providing enough data for the determination of the relative stereochemistry. Copyright © 2005 John Wiley & Sons, Ltd.
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