Study of geometric isomerism of ethyl β-aryl(hetaryl)-α-nitroacrylates by 1H NMR spectroscopy method
- Authors: Baichurin R.I.1, Berestovitskaya D.B.1, Baichurina L.V.2, Aboskalova N.I.1, Berestovitskaya V.M.1
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Affiliations:
- Herzen State Pedagogical University of Russia
- Kirov Military Medical Academy
- Issue: Vol 86, No 1 (2016)
- Pages: 51-57
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/213414
- DOI: https://doi.org/10.1134/S1070363216010102
- ID: 213414
Cite item
Abstract
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 1H NMR spectroscopy.
About the authors
R. I. Baichurin
Herzen State Pedagogical University of Russia
Author for correspondence.
Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186
D. B. Berestovitskaya
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186
L. V. Baichurina
Kirov Military Medical Academy
Email: kohrgpu@yandex.ru
Russian Federation, St. Petersburg
N. I. Aboskalova
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186
V. M. Berestovitskaya
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186