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Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols. / Zhu, Zhongwei; Koltunov, Konstantin Yu.

In: Mendeleev Communications, Vol. 30, No. 2, 01.03.2020, p. 190-191.

Research output: Contribution to journal › Article › peer-review

Harvard

Zhu, Z & Koltunov, KY 2020, 'Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols', Mendeleev Communications, vol. 30, no. 2, pp. 190-191. https://doi.org/10.1016/j.mencom.2020.03.020

APA

Zhu, Z., & Koltunov, K. Y. (2020). Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols. Mendeleev Communications, 30(2), 190-191. https://doi.org/10.1016/j.mencom.2020.03.020

Vancouver

Zhu Z, Koltunov KY. Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols. Mendeleev Communications. 2020 Mar 1;30(2):190-191. doi: 10.1016/j.mencom.2020.03.020

Author

Zhu, Zhongwei ; Koltunov, Konstantin Yu. / Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols. In: Mendeleev Communications. 2020 ; Vol. 30, No. 2. pp. 190-191.

BibTeX

@article{9b604c54cd1247f499f5584ea6a87095,
title = "Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols",
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.",
keywords = "5,6,7,8-tetrahydronaphthols, cyclohexane, ionic hydrogenation, naphthyl ethers, organofluorine compounds, polyfluoropyridines",
author = "Zhongwei Zhu and Koltunov, {Konstantin Yu}",
year = "2020",
month = mar,
day = "1",
doi = "10.1016/j.mencom.2020.03.020",
language = "English",
volume = "30",
pages = "190--191",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "2",

}

RIS

TY - JOUR

T1 - Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols

AU - Zhu, Zhongwei

AU - Koltunov, Konstantin Yu

PY - 2020/3/1

Y1 - 2020/3/1

N2 - 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.

AB - 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.

KW - 5,6,7,8-tetrahydronaphthols

KW - cyclohexane

KW - ionic hydrogenation

KW - naphthyl ethers

KW - organofluorine compounds

KW - polyfluoropyridines

UR - http://www.scopus.com/inward/record.url?scp=85085026298&partnerID=8YFLogxK

U2 - 10.1016/j.mencom.2020.03.020

DO - 10.1016/j.mencom.2020.03.020

M3 - Article

AN - SCOPUS:85085026298

VL - 30

SP - 190

EP - 191

JO - Mendeleev Communications

JF - Mendeleev Communications

SN - 0959-9436

IS - 2

ER -

ID: 24391195