Ionic Hydrogenation of Naphthyl Tetrafluoropyridin-4-yl Ethers as a New Route to 5,6,7,8-tetrahydronaphthols | Sciact - CRIS-system of Boreskov Institute of Catalysis

Ionic Hydrogenation of Naphthyl Tetrafluoropyridin-4-yl Ethers as a New Route to 5,6,7,8-tetrahydronaphthols ArticleGenre_short.SHORT_COMMUNICATION

Journal

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

Output data

Year: 2020, Volume: 30, Number: 2, Pages: 190-191 Pages count : 2 DOI: 10.1016/j.mencom.2020.03.020

Tags

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

Authors

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

Affiliations

1	Department of Natural Sciences, Novosibirsk State University, 630090 Novosibirsk, Russian Federation
2	G. K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

Funding (1)

Federal Agency for Scientific Organizations

0303-2016-0006 (V.44.1.6)

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.

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. V.30. N2. P.190-191. DOI: 10.1016/j.mencom.2020.03.020 WOS Scopus РИНЦ AN OpenAlex

Submitted:	Sep 27, 2019
Published print:	Apr 1, 2020
Published online:	May 21, 2020

Web of science:	WOS:000536145700020
Scopus:	2-s2.0-85085026298
Elibrary:	43285680
Chemical Abstracts:	2020:1021674
OpenAlex:	W3027332592

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