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Research on perinone compounds

V. Formation of 10- and 11-substituted naphthaloperinones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

11-Substituted 14H-benz[4,5]isoquinolino[2,1-a]perimidin-14-ones were synthesized, and their spectra were studied. In contrast to electron-acceptor substituents, electron-donor substituents have little effect on the shift of the absorption maxima. In the reactions of 1,8-naphthalenediamine with various 4-substituted naphthalic anhydrides, electron-donor substituents have little effect on the shift of the absorption maxima. In the reactions of 1,8-naphthalenediamine with various 4-substituted naphthalic anhydrides, electron-donor substituents lead primarily to 10-substituted naphthaloperinones, whereas electron-acceptor substituents lead primarily to 11-substituted naphthaloperinones. An assumption regarding the mechanism of the formation of 10- and 11-substituted naphthaloperinones is expressed.

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Authors and Affiliations

  1. Rubezhnoe Branch, Scientific-Research Institute of Organic Intermediates and Dyes, USSR

    V. I. Tikhonov & V. I. Rogovik

Authors
  1. V. I. Tikhonov
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  2. V. I. Rogovik
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Additional information

See [1] for communication IV.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1649–1654, December, 1974.

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Tikhonov, V.I., Rogovik, V.I. Research on perinone compounds. Chem Heterocycl Compd 10, 1450–1454 (1974). https://doi.org/10.1007/BF00474327

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  • DOI: https://doi.org/10.1007/BF00474327

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