## Abstract The ^13^C NMR spectrum (at natural abundance) of monomeric chlorophyll α in acetone‐__d__~6~ has been recorded to re‐examine the assignments of the low field (aromatic‐olefinic) region of the spectrum. The assignments, made by the examination of the fully coupled spectrum and by the use
On the assignment of the carbon-13 NMR spectrum of bilirubin
✍ Scribed by Doron Kaplan; Gil Navon
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 389 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
An individual assignment of certain peaks in the proton and ^13^C NMR spectra of bilirubin and of bilirubin dimethyl ester is described. The assignment was achieved through the spectra of vinylneoxanthobilirubinic acid and by off‐resonance decoupled ^13^C spectra of bilirubin dimethyl ester. The signals due to the endo and exo vinyl groups were separately assigned. This assignment allows a rational interpretation of previously obtained spin‐lattice relaxation times of the vinyl carbon peaks. The two vinyl groups are found to differ considerably in their motional correlation time.
📜 SIMILAR VOLUMES
## Abstract Two conflicting assignments have been proposed for the ^13^C NMR signals of 3′,5′‐cyclic nucleotides. This communication describes selective decoupling experiments for several cyclic nucleotides which provide the correct assignment based on unambiguous experimental evidence.
## Abstract The ^13^C NMR spectrum of dimethoxybilirubin dimethyl ester (1) is reported. Methoxyvinylneoxanthobilirubinic acid methyl ester, a compound containing one __endo__‐vinylpyrromethene unit, was prepared and used in the assignment of the spectrum of 1.
## Abstract The ^13^C NMR spectrum of anisomycin and the ^1^H and ^13^C NMR spectra of deacetylanisomycin were assigned using one‐ and two‐dimensional NMR analysis. The techniques included INEPT, ^1^H^13^C HETCORR and ^1^H‐^1^H COSY spectroscopy.
Using two-dimensional heteronuclear 'H-13C chemical shift correlation spectroscopy via one-bond and long-range couplings, all 13C resonances of bilirubinl X a and its dimethyl ester in dimethyl sulphoxide solution are assigned, independently from reference to partial structures. Previous ambiguities