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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2016 Volume 26, Issue 1, Pages 79–80 (Mi mendc2118)

This article is cited 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.

Language: English

DOI: 10.1016/j.mencom.2016.01.031



© Steklov Math. Inst. of RAS, 2025