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Mendeleev Communications, 1996, Volume 6, Issue 5, Pages 189–190
DOI: https://doi.org/10.1070/MC1996v006n05ABEH000638
(Mi mendc4972)
 

This article is cited in 10 scientific papers (total in 10 papers)

Condensation of acetylnaphthols with trifluoro- and trichloro-acetonitriles. The first example of ring-chain isomerism in the aromatic β-hydroxyoxoenamine series

V. Ya. Sosnovskikh

Department of Chemistry, Ural Federal University, Ekaterinburg, Russian Federation
Abstract: In contrast to 2-acetylnaphth-l-ol, condensation of l-acetylnaphth-2-ol with trifluoro- and trichloro-acetonitriles does not stop at ring-opening of the hydroxyoxoenamine form, but leads instead to 2-amino-2-trifluoro(trichloro)methyl-5,6-benzo-4-chromanones.
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Document Type: Article
Language: English


Citation: V. Ya. Sosnovskikh, “Condensation of acetylnaphthols with trifluoro- and trichloro-acetonitriles. The first example of ring-chain isomerism in the aromatic β-hydroxyoxoenamine series”, Mendeleev Commun., 6:5 (1996), 189–190
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  • https://www.mathnet.ru/eng/mendc/v6/i5/p189
  • This publication is cited in the following 10 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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