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Mendeleev Communications, 1998, Volume 8, Issue 6, Pages 242–243
DOI: https://doi.org/10.1070/MC1998v008n06ABEH001017 (Mi mendc4749) 		 
This article is cited in 12 scientific papers (total in 12 papers)

Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines

M. A. Mironov, V. S. Mokrushin

Department of Technology of Organic Synthesis, Urals State Technical University, Ekaterinburg, Russian Federation
Full-text PDF (162 kB) Citations (12)
DOI: https://doi.org/10.1070/MC1998v008n06ABEH001017
Abstract: A new reaction between aromatic isocyanides containing electron-withdrawing substituents and triethylamine is described which allows 2-triethylammonium-3-arylaminoindolates to be obtained. The structure of the compounds was determined by X-ray analysis, NMR and mass spectroscopy
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Document Type: Article
Language: English


Citation: M. A. Mironov, V. S. Mokrushin, “Reaction of aromatic isocyanides with triethylamine: a new method for the synthesis of indole betaines”, Mendeleev Commun., 8:6 (1998), 242–243
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  • https://www.mathnet.ru/eng/mendc/v8/i6/p242
    • This publication is cited in the following 12 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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