Generation of electrophilic iodine from iodine monochloride in neutral media. Iodination and protodeiodination of carbazone / V. D. Filimonov, E. A. Krasnokutskaya, Yu. A. Lesina

Уровень набора: Russian Journal of Organic Chemistry = 1956-Основной Автор-лицо: Filimonov, V. D., Russian chemist, Professor of the TPU, 1945-, Viktor Dmitrievich, 070Альтернативный автор-лицо: Krasnokutskaya, E. A., 070;Lesina, Yu. A., 070Язык: английский.Страна: .Резюме или реферат: In reaction of iodine monochloride with CF3COOAg, CH 3COONa or (CH3COO)2Pb in acetonitrile and acetic acid the chloride is bonded by metal cations, and electrophilic iodine is generated able to easily iodinate anthracene and carbazole. However at the iodination of anthracene in the presence of oxygen the prevailing process is anthracene oxidation to anthraquinone. In the presence of sulfuric acid protodeiodination of 3-iodocarbazole was found to occur resulting in rearranged products..Аудитория: .Тематика: труды учёных ТПУ
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In reaction of iodine monochloride with CF3COOAg, CH 3COONa or (CH3COO)2Pb in acetonitrile and acetic acid the chloride is bonded by metal cations, and electrophilic iodine is generated able to easily iodinate anthracene and carbazole. However at the iodination of anthracene in the presence of oxygen the prevailing process is anthracene oxidation to anthraquinone. In the presence of sulfuric acid protodeiodination of 3-iodocarbazole was found to occur resulting in rearranged products.

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