A Convenient Synthesis of 8-Hydroxy-1-Tetralones from Naphthalene-1,8-Diol | Sciact - CRIS-system of Boreskov Institute of Catalysis

A Convenient Synthesis of 8-Hydroxy-1-Tetralones from Naphthalene-1,8-Diol Full article

Journal

Mendeleev Communications
ISSN: 0959-9436 , E-ISSN: 1364-551X

Output data

Year: 2016, Volume: 26, Number: 1, Pages: 79-80 Pages count : 2 DOI: 10.1016/j.mencom.2016.01.031

Tags

ALUMINUM HALIDES1-NAPHTHOL DERIVATIVES; AROMATIC-COMPOUNDS; ACIDIC AGENTS; CONDENSATION; NAPHTHALENE; DIOLS; CYCLOHEXANE; BENZENE; PHENOLS

Authors

Zhu Zhongwei ^1,2 , Koltunov Konstantin Yu. ^1,3

Affiliations

1	Department of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russian Federation
2	Heilongjiang University, Nan-gang, Harbin, 150080, P. R. China
3	G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

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.

Zhu Z. , Koltunov K.Y.
A Convenient Synthesis of 8-Hydroxy-1-Tetralones from Naphthalene-1,8-Diol
Mendeleev Communications. 2016. V.26. N1. P.79-80. DOI: 10.1016/j.mencom.2016.01.031 WOS Scopus РИНЦ ANCAN OpenAlex

Submitted:	Apr 27, 2015
Published print:	Jan 1, 2016
Published online:	Feb 2, 2016

Web of science:	WOS:000370901100031
Scopus:	2-s2.0-84995784200
Elibrary:	27574054
Chemical Abstracts:	2016:212429
Chemical Abstracts (print):	164:238784
OpenAlex:	W2267828755

DB	Citing
Web of science	3
Scopus	3
Elibrary	2
OpenAlex	5