Synthesis and Structure of Geminally Activated 1-Nitro-4-phenylbuta-1,3-dienes


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Abstract

The condensation of cinnamaldehyde with nitro-substituted CH acids (ethyl nitroacetate, nitroacetone, nitroacetophenone, and nitroacetonitrile) afforded a series of geminally activated 1-nitro-4-phenylbuta- 1,3-dienes. Their structure was determined on the basis of a set of 1H, 13C–{1H}, 15N NMR, and IR spectra.

About the authors

R. I. Baichurin

Herzen State Pedagogical University of Russia

Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186

L. M. Alizada

Herzen State Pedagogical University of Russia

Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186

N. I. Aboskalova

Herzen State Pedagogical University of Russia

Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186

S. V. Makarenko

Herzen State Pedagogical University of Russia

Author for correspondence.
Email: kohrgpu@yandex.ru
Russian Federation, nab. reki Moiki 48, St. Petersburg, 191186

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