D. Yu. Razorenov, S. A. Makulova, I. V. Fedyanin, K. A. Lyssenko, K. M. Skupov, Yu. A. Volkova, I. I. Ponomarev, I. I. Ponomarev, “Diimidazo[4,5-b:4′,5′-e]pyridine: synthesis and nucleophilic aromatic substitution reaction”, Mendeleev Commun., 29:2 (2019), 181

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Mendeleev Communications, 2019, Volume 29, Issue 2, Pages 181–183
DOI: https://doi.org/10.1016/j.mencom.2019.03.022 (Mi mendc1464)

This article is cited in 3 scientific papers (total in 3 papers)

Communications

Diimidazo[4,5-b:4′,5′-e]pyridine: synthesis and nucleophilic aromatic substitution reaction

D. Yu. Razorenov, S. A. Makulova, I. V. Fedyanin, K. A. Lyssenko, K. M. Skupov, Yu. A. Volkova, I. I. Ponomarev, I. I. Ponomarev

A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation

Full-text PDF (675 kB) Citations (3) Supplementary materials

DOI: https://doi.org/10.1016/j.mencom.2019.03.022

Graphic abstract: Diimidazo[4,5-<i>b</i>:4′,5′-<i>e</i>]pyridine: synthesis and nucleophilic aromatic substitution reaction

Abstract: 1,7-Dihydrodiimidazo[4,5-b:4′,5′-e]pyridine obtained by reductive heterocyclization was N-arylated with 4-fluoronitrobenzene to form two regioisomers in 7 : 3 ratio. This N-arylation is considered as a model reaction for the polymer synthesis.

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Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(1.7 Mb)

Citation: D. Yu. Razorenov, S. A. Makulova, I. V. Fedyanin, K. A. Lyssenko, K. M. Skupov, Yu. A. Volkova, I. I. Ponomarev, I. I. Ponomarev, “Diimidazo[4,5-b:4′,5′-e]pyridine: synthesis and nucleophilic aromatic substitution reaction”, Mendeleev Commun., 29:2 (2019), 181–183

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https://www.mathnet.ru/eng/mendc/v29/i2/p181

This publication is cited in the following 3 articles:

Citing articles in Google Scholar: Russian citations, English citations
Related articles in Google Scholar: Russian articles, English articles

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