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Nucleophilic Transformations of Heterocyclic Derivatives of 4-Heteryl-2,4-dioxobutanoic Acids

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Abstract

Proceeding from 4-heteryl-2,4-dioxobutanoic acids were prepared (Z)-3-heteroylmethylene-1,2,3,4-tetrahydro-2-quinoxalones that when treated with oxalyl chloride afforded 3-heteroyl-1,2,4,5-tetrahydropyrrolo[1,2-a]quinoxaline-1,2,4-triones. The latter took in reactions with o-aminophenol and o-phenylenediamine two different directions.

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Authors and Affiliations

  1. Institute of Technical Chemistry, Ural Division, Russian Academy of Sciences, Perm, 614600, Russia

    I. A. Tolmacheva, I. V. Mashevskaya & A. N. Maslivets

  2. Perm State University, Perm, 614600, Russia

    I. A. Tolmacheva, I. V. Mashevskaya & A. N. Maslivets

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  1. I. A. Tolmacheva
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  2. I. V. Mashevskaya
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  3. A. N. Maslivets
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Tolmacheva, I.A., Mashevskaya, I.V. & Maslivets, A.N. Nucleophilic Transformations of Heterocyclic Derivatives of 4-Heteryl-2,4-dioxobutanoic Acids. Russian Journal of Organic Chemistry 38, 281–285 (2002). https://doi.org/10.1023/A:1015590306099

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