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Title: /sup 13/C NMR spectra of cyclic nitrones. 2. 1- and 4-substituted 2,2,5,5-tetramethyl-3-imidazoline 3-oxides

Journal Article · · Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00504212· OSTI ID:6181311

The chemical shift of the carbon atom of the nitrone group in the /sup 13/C NMR spectra of 3-imidazoline 3-oxides lies in the region of 117-152 ppm and depends on the electronic effect of the substituents at positions 1, 4, and 5 of the heterocycle. Increase in the electron-withdrawing character of the substituent at these positions leads to an upfield shift of the signal for the nitrone carbon atom, and this corresponds to the increase in electron density on it.

Research Organization:
Novosibirsk Institute of Organic Chemistry, USSR
OSTI ID:
6181311
Journal Information:
Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Vol. 21:2; Other Information: Translated from Khim. Geterotsikl. Soedin.; 21: No.2, 252-259(Feb 1985)
Country of Publication:
United States
Language:
English