A. S. Kiselev, A. A. Gakh, A. V. Samet, V. V. Semenov, “Aromatic Ring Opening of Pyridinium Salts using Carbanions formed from Malononitrile and Ethyl Cyanoacetate”, Mendeleev Commun., 1992, Volume 2, Issue 1,Pages <nobr>25

This article is cited in 4 papers

Aromatic Ring Opening of Pyridinium Salts using Carbanions formed from Malononitrile and Ethyl Cyanoacetate

A. S. Kiselev, A. A. Gakh, A. V. Samet, V. V. Semenov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Carbanions formed from malononitrile and ethyl cyanoacetate have been found to react with pyridinium salts via ring-opening to form 1,1,7,7-tetrasubstituted hepta-1,3,5-trienes.

Language: English

DOI: 10.1070/MC1992v002n01ABEH000108