Аннотация:
Naphthalene-1,8-diol on superelectrophilic activation with aluminium halides smoothly reacts with cyclohexane and benzene to afford 8-hydroxy-1-tetralone and 8-hydroxy-4-phenyl-1-tetralone, respectively.
Образец цитирования:
Zh. Zhu, K. Yu. Koltunov, “A convenient synthesis of 8-hydroxy-1-tetralones from naphthalene-1,8-diol”, Mendeleev Commun., 26:1 (2016), 79–80
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2118
https://www.mathnet.ru/rus/mendc/v26/i1/p79
Эта публикация цитируется в следующих 3 статьяx:
J. Irshad Ahamed, S.I. Davis Presley, Jothi Ramalingam Rajabathar, V.O. Sangeetha, Venkatadri Babu, Manickam Rajkumar, Manjunath S. Kamath, “Analyze and assess the spectral, DFT, and medicinal characteristics through targeted pharmacological investigation of 2-(3-(5-(4-chlorophenyl)furan-2-yl)acryloyl)-3,4-dihydro-2H-naphthalen-1-one (CHFADN)”, Journal of Molecular Structure, 1321 (2025), 139659
Douglas A. Klumpp, Maksim V. Anokhin, “Superelectrophiles: Recent Advances”, Molecules, 25:14 (2020), 3281
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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