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 w
1H and 13C chemical shifts and coupling constants of lupane. Application of two-dimensional NMR techniques
✍ Scribed by Willi Ammann; René Richarz; Toni Wirthlin; Detlef Wendisch
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 505 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
2D NMR techniques (J‐resolved ^13^C, ^13^C^13^C correlated, ^1^H^13^C correlated) were used to gather more chemical shift and coupling information on the pentacyclic triterpene, lupane. They confirm and complete ^13^C assignments made earlier, and corroborate the constitution and major configurational details of lupane. Lupane is a parent compound and spectral reference in the study of sedimental demethylated triterpenes.
📜 SIMILAR VOLUMES
The NMR parameters characterizing the spectra of trans- and cis-decalins were determined from theoretical calculations and experimental spectra. The calculated values of the shielding constants are in good agreement with the measured chemical shifts, with a small but noticeable difference in accurac
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
## 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
The attachment of an ester group at C-4 (1) and lactone bridges between C-6 and C-8 (1); C-2 and C-4, C-6 and C-8 (2); C-4 and C-6 (4) resulted in C-4, C-5 and C-6 showing similar chemical shifts in all three structures. In Diosbulbins A (1) and B (Z), C-12 bearing the equatorial furan ring is in an