Epimeric mixtures of isoHazolidine derivatives were investigated by ' H NMR spectra obtained in the presence of lanthanide shift reagents. The NMR signals of all the components contained in a mixture of 2 , 3 -d i p n e n y l -S -c e ~y ~~~~e s were identified and the LISCA computer program enabled
Conformational studies of some 2-phenylpropyl derivatives by NMR spectroscopy and use of lanthanide shift reagents
β Scribed by S.L. Spassov; R. Stefanova
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 473 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-2860
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π SIMILAR VOLUMES
The 13C NMR behaviour of ten acyclic terpene alcohols was examined in the presence of a chiral lanthanide shift reagent (CLSR). For each alcohol, we measured the lanthanide-induced shift (LIS) on the signals of the carbons and the splitting of some signals, which allowed the enantiomeric differentia
## Abstract The ^13^C chemical shift of the substituted or functionalized carbon of various medium and large rings is plotted against ring size (6β15 carbons). The curves thus obtained allow a conformational analysis of the corresponding derivatives.
The conformational analysis of short polymer chains involves the use of statistical models, and their predictions must be checked against experimental information. Ytterbium-induced shifts in the "C NMR spectra of fatty acids provide a non-perturbing, straightforward method of simultaneously obtaini
of the following in a volume of 1 liter: naphthalene (150 g), 2,5-diphenyloxazole (8 g), 1,4-bis(4-methyl-5-phenyl-oxazol-2-yI)benzene (0.6 g), ethylene glycol (20 ml), 2-ethoxyethanol(lOO ml), and toluene to make 1 liter. The radioactivity was measured in the liquid scintillation counter with an 18