## 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 three sesquiterpenoids from Inula helenium
✍ Scribed by Yan Huo; Haiming Shi; Mengyue Wang; Prof. Xiaobo Li
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 95 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2340
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✦ Synopsis
Abstract
The complete assignments of all the ^1^H and ^13^C NMR signals of three sesquiterpene lactones, 4‐oxo‐5(6),11‐eudesmadiene‐8,12‐olide (1), 4‐oxo‐11‐eudesmaene‐8,12‐olide (2) and (1(10)E)‐5β‐Hydroxygermacra‐1(10),4(15),11‐trien‐8, 12‐olide (3), were carried out by various 2D NMR experiments. Compounds 1–3 were isolated from the roots of Inula helenium for the first time. Among them, 1 was identified as a new nor‐sesquiterpene lactone, and 2 was isolated from a natural source for the first time. The ^13^C‐NMR data of compound 3 was also reported for the first time. Copyright © 2008 John Wiley & Sons, Ltd.
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