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This article is cited in 9 scientific papers (total in 9 papers)
Alkylation of deactivated arenes by alkanes in the presence of aprotic organic superacid CBr4·2AlBr3
A. V. Orlinkov, I. S. Akhrem, L. V. Afanas'eva, E. I. Mysov, M. E. Vol'pin
A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
Deactivated arenes (di- and tri-halobenzenes, acetophenone, benzophenone and methylbenzoate) have been shown to be alkylated by alkanes and cycloalkanes (propane, n-butane, cyclopentane) in the presence of superacid CBr4·2AlBr3 in the range –40 to 0 °C; in some cases selective and effective mono- or di-alkylation can be achieved.
Citation:
A. V. Orlinkov, I. S. Akhrem, L. V. Afanas'eva, E. I. Mysov, M. E. Vol'pin, “Alkylation of deactivated arenes by alkanes in the presence of aprotic organic superacid CBr4·2AlBr3”, Mendeleev Commun., 7:2 (1997), 61–63
Linking options:
https://www.mathnet.ru/eng/mendc4783 https://www.mathnet.ru/eng/mendc/v7/i2/p61
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