Mendeleev Commun., 2020 Volume 30, Issue 2, Pages 190–191
(Mi mendc1144)
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2 papers
Communications Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols Zh. Zhu a ,
K. Yu. Koltunov ab a Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation b G.K. Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation 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:
polyfluoropyridines, naphthyl ethers, ionic hydrogenation, 5,6,7,8-tetrahydronaphthols, organofluorine compounds, cyclohexane.
Language: English
DOI:
10.1016/j.mencom.2020.03.020
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