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


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

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


Copyright (c) 2018 Pleiades Publishing, Ltd.

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies