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

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Zhu Z., Koltunov K. Y. A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 79-80.
GOST all authors (up to 50) Copy
Zhu Z., Koltunov K. Y. A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 79-80.
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TY - JOUR
DO - 10.1016/j.mencom.2016.01.031
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.031
TI - A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol
T2 - Mendeleev Communications
AU - Zhu, Zhongwei
AU - Koltunov, Konstantin Yurievich
PY - 2015
DA - 2015/12/30
PB - Mendeleev Communications
SP - 79-80
IS - 1
VL - 26
ER -
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@article{2015_Zhu,
author = {Zhongwei Zhu and Konstantin Yurievich Koltunov},
title = {A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol},
journal = {Mendeleev Communications},
year = {2015},
volume = {26},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.031},
number = {1},
pages = {79--80},
doi = {10.1016/j.mencom.2016.01.031}
}
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Zhu, Zhongwei, and Konstantin Yurievich Koltunov. “A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol.” Mendeleev Communications, vol. 26, no. 1, Dec. 2015, pp. 79-80. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.031.

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.

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