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Oxidative arylamination of 1,7-dihydroxynaphthalene

  • Organic Chemistry
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Russian Chemical Bulletin Aims and scope

Abstract

1,7-Dihydroxynaphthalene reacts with aniline orp-toluidine in the presence of oxidants to give the correspondingN-aryl-7-hydroxy-1,4-naphthoquinone 4-imines, 2-arylamino- and 2,8-diarylamino-N-aryl-7-hydroxy-1,4-naphthoquinone 4-imines, and benzo[a]oxophenoxazinimine derivatives.

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Authors and Affiliations

  1. Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp. Akad. Lavrent'eva, 630090, Novosibirsk, Russian Federation

    L. V. Ektova

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  1. L. V. Ektova
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Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 347–350, February, 1999.

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Ektova, L.V. Oxidative arylamination of 1,7-dihydroxynaphthalene. Russ Chem Bull 48, 346–349 (1999). https://doi.org/10.1007/BF02494562

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  • DOI: https://doi.org/10.1007/BF02494562

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