Synthesis of Geminally Activated 4-(Furan-2-yl)- and 4-(Thiophen-2-yl)-1-nitrobuta-1,3-dienes
- Authors: Baichurin R.I.1, Reshetnikov A.A.1, Sergeev V.D.1, Aboskalova N.I.1, Makarenko S.V.1
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Affiliations:
- Herzen State Pedagogical University of Russia
- Issue: Vol 89, No 5 (2019)
- Pages: 865-869
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222891
- DOI: https://doi.org/10.1134/S1070363219050025
- ID: 222891
Cite item
Abstract
The condensation of 3-(furan-2-yl)- and 3-(thiophen-2-yl)prop-2-enals with nitro-substituted CH acids, namely ethyl nitroacetate, nitroacetone, nitroacetophenone, and nitroacetonitrile, afforded a series of geminally activated nitro dienes, 4-(furan-2-yl)- and 4-(thiophen-2-yl)-1-nitrobuta-1,3-dienes. The product structure was confirmed by NMR and IR spectroscopy.
About the authors
R. I. Baichurin
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Russian Federation, nab. r. Moiki 48, St. Petersburg, 191186
A. A. Reshetnikov
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Russian Federation, nab. r. Moiki 48, St. Petersburg, 191186
V. D. Sergeev
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Russian Federation, nab. r. Moiki 48, St. Petersburg, 191186
N. I. Aboskalova
Herzen State Pedagogical University of Russia
Email: kohrgpu@yandex.ru
Russian Federation, nab. r. Moiki 48, St. Petersburg, 191186
S. V. Makarenko
Herzen State Pedagogical University of Russia
Author for correspondence.
Email: kohrgpu@yandex.ru
Russian Federation, nab. r. Moiki 48, St. Petersburg, 191186