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Mendeleev Communications, 1992, Volume 2, Issue 1, Pages 25–26
DOI: https://doi.org/10.1070/MC1992v002n01ABEH000108 (Mi mendc5379) 		 
This article is cited in 4 scientific papers (total 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
Full-text PDF (227 kB) Citations (4)
DOI: https://doi.org/10.1070/MC1992v002n01ABEH000108
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.
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Document Type: Article
Language: English


Citation: 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., 2:1 (1992), 25–26
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    • This publication is cited in the following 4 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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