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Mendeleev Communications, 2001, Volume 11, Issue 2, Pages 77–78
DOI: https://doi.org/10.1070/MC2001v011n02ABEH001380 (Mi mendc4226) 		 
This article is cited in 3 scientific papers (total in 3 papers)

Regioselectivity in the reactions of pyrroles with 3-aryl-1,2,4-triazin-5-ones

O. N. Chupakhina, V. L. Rusinovb, G. V. Zyryanovb

a I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
Full-text PDF (76 kB) Citations (3)
DOI: https://doi.org/10.1070/MC2001v011n02ABEH001380
Abstract: Depending on the nature of acylating agents, the reaction of 1-methylpyrrole with 3-aryl-1,2,4-triazin-5-ones leads to either α- or β-heteroarylpyrroles with a high degree of regioselectivity.
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Document Type: Article
Language: English


Citation: O. N. Chupakhin, V. L. Rusinov, G. V. Zyryanov, “Regioselectivity in the reactions of pyrroles with 3-aryl-1,2,4-triazin-5-ones”, Mendeleev Commun., 11:2 (2001), 77–78
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  • https://www.mathnet.ru/eng/mendc/v11/i2/p77
    • This publication is cited in the following 3 articles:
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