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., 2019, Volume 29, Issue 2,Pages 181

This article is cited 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

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.

Language: English

DOI: 10.1016/j.mencom.2019.03.022

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