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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. Zhu
ab
,
K. Yu. Koltunov
ac
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
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