Study of geometric isomerism of ethyl β-aryl(hetaryl)-α-nitroacrylates by 1H NMR spectroscopy method
- Авторы: Baichurin R.1, Berestovitskaya D.1, Baichurina L.2, Aboskalova N.1, Berestovitskaya V.1
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Учреждения:
- Herzen State Pedagogical University of Russia
- Kirov Military Medical Academy
- Выпуск: Том 86, № 1 (2016)
- Страницы: 51-57
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/213414
- DOI: https://doi.org/10.1134/S1070363216010102
- ID: 213414
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Аннотация
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.
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Об авторах
R. Baichurin
Herzen State Pedagogical University of Russia
Автор, ответственный за переписку.
Email: kohrgpu@yandex.ru
Россия, nab. reki Moiki 48, St. Petersburg, 191186
D. Berestovitskaya
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Россия, nab. reki Moiki 48, St. Petersburg, 191186
L. Baichurina
Kirov Military Medical Academy
Email: kohrgpu@yandex.ru
Россия, St. Petersburg
N. Aboskalova
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Россия, nab. reki Moiki 48, St. Petersburg, 191186
V. Berestovitskaya
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Россия, nab. reki Moiki 48, St. Petersburg, 191186
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