## Abstract Granatin B, a complex ellagitannin extracted from pomegranate fruit, has two equilibrating isomers, form a and form b. A full ensemble of proton and carbon‐13 NMR methods over a wide range of temperature enabled a complete assignment of the more abundant isomer and showed it to be form
NMR of anthocyanins: Assignments and effects of exchanging aromatic protons
✍ Scribed by Atle T. Pedersen; Øyvind M. Andersen; Dagfinn W. Aksnes; Willy Nerdal
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 459 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Pelargonidin‐3‐O‐β‐glucopyranoside was isolated from an acidified methanolic extract of frozen strawberries, purified by several chromatographical techniques and subjected to homo‐ and heteronuclear proton and carbon NMR analysis, including selective decoupling, DQF‐COSY, NOESY, SEFT, HMQC and HMBC. Several strategies for the unambiguous assignment of the aglycone H‐6 and H‐8 resonances are discussed. Secondary isotope effects and different deuterium exchange rates of the protons were found.
📜 SIMILAR VOLUMES
## Abstract The ^1^H and ^13^C NMR spectra of pentalongin, a physiologically active natural product, were completely assigned. Some previous assignments were revised. All ^13^C^1^H coupling constants, both one‐bond and long‐range, were also measured.
Several one-and two-dimensional techniques have been used to assign the 'H and "C NMR spectra of the cyclic heptadepsipeptide didemnin A in DMSO. The composition and sequence of the amino acid residues was known beforehand and could be confirmed by heteronuclear proton-carbon long-range couplings us
## Abstract The ^1^H and ^13^C NMR spectra of 5‐acetyl‐7,4′‐dimethoxyflavone‐(6–8″)‐5″‐acetyl‐7″,4‴‐dimethoxyflavone, a new agathisflavone derivative, were completely assigned on the basis of 1D and 2D NMR techniques. Copyright © 2005 John Wiley & Sons, Ltd.