## 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 a novel diterpenoid from Semiaquilegia adoxoides
✍ Scribed by Feng Niu; Zheng Cui; Qin Li; Haitao Chang; Yong Jiang; Liang Qiao; Peng-fei Tu
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 85 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1812
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✦ Synopsis
Abstract
Semiaquilegoside A (1), a new diterpenoid, was isolated from the roots of Semiaquilegia adoxoides. Its chemical structure was established as 3β, 11‐ dihydroxy‐12‐O‐β‐D‐glucopyranosyl‐8,11,13‐abietatrien‐6‐one through spectroscopic techniques and chemical analysis. Copyright © 2006 John Wiley & Sons, Ltd.
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