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100 _a20110630a2003 k y0engy50 ba
101 0 _aeng
102 _aUS
200 1 _aGeneration of electrophilic iodine from iodine monochloride in neutral media. Iodination and protodeiodination of carbazone
_fV. D. Filimonov, E. A. Krasnokutskaya, Yu. A. Lesina
330 _aIn 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.
333 _aВ фонде НТБ ТПУ отсутствует
461 _tRussian Journal of Organic Chemistry
_d1956-
463 _tVol. 39, № 6
_vP. 875-880
_d2003
610 1 _aтруды учёных ТПУ
700 1 _aFilimonov
_bV. D.
_cRussian chemist
_cProfessor of the TPU
_f1945-
_gViktor Dmitrievich
_xTPU
_2stltpush
_3(RuTPU)RU\TPU\pers\26423
_4070
701 1 _aKrasnokutskaya
_bE. A.
_4070
701 1 _aLesina
_bYu. A.
_4070
801 1 _aRU
_b63413507
_c20100928
801 2 _aRU
_b63413507
_c20140131
_gRCR
942 _cBK