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Polyfunctional imidazoles: II. Synthesis and reactions with nucleophilic reagents of 1-substituted 2,4-dichloro-1H-imidazole-5-carbaldehydes

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dc.contributor.author Chornous, V.A.
dc.contributor.author Grozav, A.N.
dc.contributor.author Rusanov, E.B.
dc.contributor.author Nesterenko, A.M.
dc.contributor.author Vovk, M.V.
dc.date.accessioned 2012-06-27T19:33:00Z
dc.date.available 2012-06-27T19:33:00Z
dc.date.issued 2011
dc.identifier.uri http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/2343
dc.description.abstract 1-Alkyl(aryl)imidazolidine-2,4-diones reacted with Vilsmeier-Haack reagent affording 1-alkyl(aryl)-2,4-dichloro-1H-imidazole-5-carbaldehydes whose reactions with sodium azide, sodium alkoholates, with phenols, thiols, and secondary cycloalkylamines led to the substitution of chlorine in the position 2 of the imidazole ring. The reaction with primary amines resulted in the condensation products at the aldehyde group. ru_RU
dc.language.iso en ru_RU
dc.publisher Russian Journal of Organic Chemistry ru_RU
dc.title Polyfunctional imidazoles: II. Synthesis and reactions with nucleophilic reagents of 1-substituted 2,4-dichloro-1H-imidazole-5-carbaldehydes ru_RU
dc.type Article ru_RU


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