1-(Benzimidazol-2-yl)-1,2-dioxoalkane arylhydrazones and 2-phenylbenzimidazole as the main products of the reactions of 1,2,3-triketone 2-arylhydrazones with o-phenylenediamine

The reactions of o-phenylenediamine with 1,2,3-triketone 2-arylhydrazones containing alkyl substituents result in the predominant formation of 1-(benzimidazol-2-yl)-1,2-dioxoalkane arylhydrazones, whereas phenyl-substituted analogues afford 2-phenylbenzimidazole.

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Veröffentlicht in:Mendeleev communications 2003, Vol.13 (5), p.228-229
Hauptverfasser: Khudina, Ol’ga G., Murashova, Natal’ya V., Burgart, Yanina V., Saloutin, Viktor I.
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container_end_page 229
container_issue 5
container_start_page 228
container_title Mendeleev communications
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creator Khudina, Ol’ga G.
Murashova, Natal’ya V.
Burgart, Yanina V.
Saloutin, Viktor I.
description The reactions of o-phenylenediamine with 1,2,3-triketone 2-arylhydrazones containing alkyl substituents result in the predominant formation of 1-(benzimidazol-2-yl)-1,2-dioxoalkane arylhydrazones, whereas phenyl-substituted analogues afford 2-phenylbenzimidazole.
doi_str_mv 10.1070/MC2003v013n05ABEH001788
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title 1-(Benzimidazol-2-yl)-1,2-dioxoalkane arylhydrazones and 2-phenylbenzimidazole as the main products of the reactions of 1,2,3-triketone 2-arylhydrazones with o-phenylenediamine
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