## Abstract Four new furostanol saponins (1–4), two pairs of diastereoisomers, were isolated from methanolic extracts of __T__upistra chinensis rhizomes and their structures were assigned from ^1^H and ^13^C NMR spectra, DEPT, and by 2D COSY, NOESY, HMQC, and HMBC experiments. Copyright © 2008 John
Isolation and identification by 2D NMR of two new complex saponins from Michrosechium helleri
✍ Scribed by Ismael León; Raul G. Enríquez; Stewart McLean; William F. Reynolds; Margaret Yu
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 240 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Two complex saponins, amole F and G, were characterized and their spectra were assigned using only 1D and 2D 1H and NMR methods. Amole F and G have seven and six monosaccharides, respectively, linked to the triterpene aglycone bayogenin. In addition to standard 2D methods, a series of TOCSY spectra with di †erent mixing times and a high-resolution coupled HSQC spectrum were particularly useful for assigning the monosaccharide units. It is concluded that saponins of this complexity are approaching the limit of structural complexity that can be solved by NMR alone, although the limit might be pushed further by access to ultra-high Ðeld NMR spectrometers.
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