Study of geometric isomerism of ethyl β-aryl(hetaryl)-α-nitroacrylates by 1H NMR spectroscopy method

Features of Z → E isomerization of ethyl α-nitrocinnamates as well as their furyl and thienyl heteroanalogs depending on the nature of the substituent in the β-position of α-nitroacrylates, deuterated solvent and duration of exposure of the sample were studied by means of 1 H NMR spectroscopy.

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Bibliographic Details
Published in:Russian journal of general chemistry 2016, Vol.86 (1), p.51-57
Main Authors: Baichurin, R. I., Berestovitskaya, D. B., Baichurina, L. V., Aboskalova, N. I., Berestovitskaya, V. M.
Format: Article
Language:English
Subjects:
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
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Summary:Features of Z → E isomerization of ethyl α-nitrocinnamates as well as their furyl and thienyl heteroanalogs depending on the nature of the substituent in the β-position of α-nitroacrylates, deuterated solvent and duration of exposure of the sample were studied by means of 1 H NMR spectroscopy.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363216010102