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Mendeleev Communications, 2016, Volume 26, Issue 1, Pages 79–80
DOI: https://doi.org/10.1016/j.mencom.2016.01.031
(Mi mendc2118)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol

Zh. Zhuab, K. Yu. Koltunovac

a Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
b Heilongjiang University, Harbin, P.R. China
c G.K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
Abstract: Naphthalene-1,8-diol on superelectrophilic activation with aluminium halides smoothly reacts with cyclohexane and benzene to afford 8-hydroxy-1-tetralone and 8-hydroxy-4-phenyl-1-tetralone, respectively.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (334.7 Kb)


Citation: Zh. Zhu, K. Yu. Koltunov, “A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol”, Mendeleev Commun., 26:1 (2016), 79–80
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  • https://www.mathnet.ru/eng/mendc2118
  • https://www.mathnet.ru/eng/mendc/v26/i1/p79
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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