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., 2001, Volume 11, Issue 2,Pages <nobr>77–78</nobr>

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Mendeleev Commun., 2001 Volume 11, Issue 2, Pages 77–78 (Mi mendc4226)

This article is cited in 3 papers

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

O. N. Chupakhin^a, V. L. Rusinov^b, G. V. Zyryanov^b

^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

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.

Language: English

DOI: 10.1070/MC2001v011n02ABEH001380

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