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Features of the reaction of heterocyclic analogs of chalcone with lanthanide shift reagents

Journal Article · · Chemistry of Heterocyclic Compounds
DOI:https://doi.org/10.1007/BF01169931· OSTI ID:241170
;  [1]
  1. Taras Shevchenko Kiev Univ. (Russian Federation)
The PMR spectra of heterocyclic analogs of 2-hydroxychalcone containing thiazole, benzofuran, triazole, imidazole, benzodioxane, or pyridine rings in the presence of lanthanide shift reagents are studied. It is found that the most effective reagent for modifying the spectra of these compounds is Yb(fod)3. The broadening of the spectra of 2-hydroxy chalcones in the presence of lanthanide shift reagents is explained by the dynamic effects of complex formation. An example is given of the determination of the conformation of molecules of 2-hydroxychalcone by the simultaneous use of lanthanide shift reagents and the homonuclear Overhauser effect. 9 refs., 1 fig., 1 tab.
Sponsoring Organization:
USDOE
OSTI ID:
241170
Journal Information:
Chemistry of Heterocyclic Compounds, Journal Name: Chemistry of Heterocyclic Compounds Journal Issue: 4 Vol. 30; ISSN 0069-3154; ISSN CHCCAL
Country of Publication:
United States
Language:
English

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