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Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols

Zhongwei Zhu 1
Zhongwei Zhu
, 
Konstantin Yurievich Koltunov 1, 2
Konstantin Yurievich Koltunov
10.1016/j.mencom.2020.03.020
Published 2020-03-02
Communication , Volume 30, Issue 2, 190-191
2
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Zhu Z., Koltunov K. Y. Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols // Mendeleev Communications. 2020. Vol. 30. No. 2. pp. 190-191.
GOST all authors (up to 50) Copy
Zhu Z., Koltunov K. Y. Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols // Mendeleev Communications. 2020. Vol. 30. No. 2. pp. 190-191.
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TY - JOUR
DO - 10.1016/j.mencom.2020.03.020
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.03.020
TI - Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols
T2 - Mendeleev Communications
AU - Zhu, Zhongwei
AU - Koltunov, Konstantin Yurievich
PY - 2020
DA - 2020/03/02
PB - Mendeleev Communications
SP - 190-191
IS - 2
VL - 30
ER -
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@article{2020_Zhu,
author = {Zhongwei Zhu and Konstantin Yurievich Koltunov},
title = {Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols},
journal = {Mendeleev Communications},
year = {2020},
volume = {30},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.03.020},
number = {2},
pages = {190--191},
doi = {10.1016/j.mencom.2020.03.020}
}
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Zhu, Zhongwei, and Konstantin Yurievich Koltunov. “Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols.” Mendeleev Communications, vol. 30, no. 2, Mar. 2020, pp. 190-191. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.03.020.

Keywords

5,6,7,8-tetrahydronaphthols
cyclohexane
ionic hydrogenation
naphthyl ethers
organofluorine compounds
polyfluoropyridines

Abstract

O-Tetrafluoropyridin-4-yl-protected naphthols undergo regioselective reduction with cyclohexane in the presence of aluminium chloride to afford the corresponding 5,6,7,8-tetrahydronaphthyl ethers.

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