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.
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/mendc1144
https://www.mathnet.ru/eng/mendc/v30/i2/p190
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