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Structures and ambiphilic reactivities of indolizines. 5. Acylation of 2-methylindolizine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The acylation and carbomethoxylation of 2-methylindolizine were studied. In most cases minor amounts of the 1-substituted isomers were isolated in addition to the “usual” products of substitution in the 3 position. The data from the PMR and mass spectra of the 2-methyl-3- and 1-acylindolizines obtained are discussed.

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Authors and Affiliations

  1. M. V. Lomonosov Moscow State University, 119899, Moscow

    S. I. Bobrovskii, D. E. Lushnikov & Yu. G. Bundel'

Authors
  1. S. I. Bobrovskii
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  2. D. E. Lushnikov
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  3. Yu. G. Bundel'
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Additional information

See [1] for Communication 4.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1634–1638, December, 1989.

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Bobrovskii, S.I., Lushnikov, D.E. & Bundel', Y.G. Structures and ambiphilic reactivities of indolizines. 5. Acylation of 2-methylindolizine. Chem Heterocycl Compd 25, 1360–1364 (1989). https://doi.org/10.1007/BF00473864

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  • DOI: https://doi.org/10.1007/BF00473864

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