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Trifluoroacetylation of 3-halo-9-methylcarbazoles
Authors:N V Moskalev  E E Sirotkina
Institution:(1) Institute of Petrochemistry, Siberian Branch, Academy of Sciences of the USSR, 634055 Tomsk
Abstract:Trifluoroacetylation of 3-halo-9-methylcarbazoles at 110DaggerC proceeds at 6-position. In the case of 3-bromo- and 3-iodo-derivatives, the reaction is complicated by competing processes of dehalogenation, followed by the halogenation of the substrate, leading to 3,6-dihalo derivatives.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1492–1495, November, 1987.
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