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Reactions of aziridine-2-carboxylic acid derivatives with esters and nitriles of unsaturated acids

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Products of addition to the multiple bond were obtained in the reaction of the methyl ester, nitrile, and amide of aziridine-2-carboxylic acid with esters or nitrides of acrylic acid and esters of maleic, acetylenemonocarboxylic, and acetylenedicarboxylic acids. The bromination of 1-(2-alkoxycarbonylethenyl)-2-methoxycarbonylaziridines under various conditions leads to the addition of bromine to the multiple bond with retention or opening of the aziridine ring.

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Authors and Affiliations

  1. Institute of Organic Synthesis, Academy of Sciences of the Latvian SSR, 226006, Riga

    P. T. Trapentsier, I. Ya. Kalvin'sh, É. É. Liepin'sh & É. Ya. Lukevits

Authors
  1. P. T. Trapentsier
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  2. I. Ya. Kalvin'sh
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  3. É. É. Liepin'sh
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  4. É. Ya. Lukevits
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 481–485, April, 1983.

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Trapentsier, P.T., Kalvin'sh, I.Y., Liepin'sh, É.É. et al. Reactions of aziridine-2-carboxylic acid derivatives with esters and nitriles of unsaturated acids. Chem Heterocycl Compd 19, 391–394 (1983). https://doi.org/10.1007/BF00516205

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  • DOI: https://doi.org/10.1007/BF00516205

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