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Mendeleev Communications, 2020, Volume 30, Issue 2, Pages 190–191
DOI: https://doi.org/10.1016/j.mencom.2020.03.020
(Mi mendc1144)
 

This article is cited in 2 scientific papers (total in 2 papers)

Communications

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

Zh. Zhua, K. Yu. Koltunovab

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.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (941.8 Kb)


Citation: Zh. Zhu, K. Yu. Koltunov, “Ionic hydrogenation of naphthyl tetrafluoropyridin-4-yl ethers as a new route to 5,6,7,8-tetrahydronaphthols”, Mendeleev Commun., 30:2 (2020), 190–191
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  • https://www.mathnet.ru/eng/mendc/v30/i2/p190
  • This publication is cited in the following 2 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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