The complete assignments of 1H and 13C NMR data for a series of synthesized diosgenyl saponin analogs are described, viz. diosgenyl b-D-glucopyranoside (1), diosgenyl a-L-rhamnopyranosyl- 7). The assignments were achieved using homo-and heteronuclear two-dimensional NMR techniques.
Complete 1H- and 13C NMR assignments of saponins from roots of Gypsophila trichotoma Wend.
โ Scribed by Reneta Gevrenova; Laurence Voutquenne-Nazabadioko; Dominique Harakat; Elise Prost; Max Henry
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 126 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1827
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โฆ Synopsis
Abstract
The assignments of ^1^H and ^13^C NMR spectra of two new aminoacyl triterpene saponins from roots of Gypsophila trichotoma Wend. are reported. In addition to 1D NMR methods, 2D NMR techniques (COSY, TOCSY, ROESY, HSQC, HMBC, and HSQCโTOCSY) were used for the assignments. The structures were completed by analysis of HRโESIโMS and ESIโMS^n^. Copyright ยฉ 2006 John Wiley & Sons, Ltd.
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