## 28B-CH3 (o'900 pprn), indicating that the 1 , y.-Z, Chen, J,-M, Yue and S,-M, Hua, 5. T. Itoh, T. Tamu'ra and T. Matsumoto, side-chain can also rotate to the front of the ## Gaodeng xuexiao Huaxue xuebao Steroids 27, 275 (1 976). molecule but is still well away from ring A
Stereochemical analysis and complete 1H/13C NMR chemical shift assignments of matrine. Application of NOE and two-dimensional NMR techniques
β Scribed by Nina C. Gonnella; Jen Chen
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 450 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
β¦ Synopsis
The stereochemical and structural analysis of matrine was carried out using nuclear magnetic resonance spectroscopy. Several methods, including ' 3C-'H two-dimensional shift correlation spectroscopy, 'H-'H two-dimensional correlated spectroscopy and measurements of vicinal 'H-'H coupling constants were used for chemical shift assignments and configurational analysis. Nuclear Overhauser effect difference spectroscopy was used to establish the sterochemistry. This investigation demonstrates the power of two-dimensional NMR techniques and the nuclear Overhauser effect (NOE) in the structural determination of natural products.
π SIMILAR VOLUMES
Twwlimensional 'H and 13C shiftcorrelated NMR experiments have been used for the unambiguous assignments of all proton and carbon chemical shifts of two cadinane and bicadinane.
H and 13C NMR signals were completely assigned for six 3a-and 6a-O-/?-~-glycosidic conjugates (glucosides, glucuronides and N-acetylglucosaminides) of hyodeoxycholic (3a,6a-dihydroxy-5/3-cholanoic) acid as their methyl ester-acetate derivatives (three being 3-glycosides and three corresponding 6-ana
The 'H and "C NMR spectra of apigeninidin chloride were assigned utilizing the two-dimensional 6,, S, correlation and COLOC and HBMC techniques. The full 13C NMR data are reported for the first time. A good correlation was found between 13C chemical shifts and carbon charge obtained by AM1 calculati
## Abstract Three prenylflavanones, sigmoidins A, B and C, were studied using oneβ and twoβdimensional NMR techniques. The interpretation of these spectra led to the definitive assignments of all carbon and hydrogen chemical shifts.
1 H and 13 C NMR spectra for seven chlorinated dibenzothiophenes (DBTs) were measured. Complete 1 H and 13 C NMR chemical shift assignments for 2, 8-and 3,7-dichloro-and 2,3,6,8-, 2,3,7,8-and 2,4,6,8-tetrachloro congeners are based on z-gradient selected inverse (proton detected) two-dimensional het