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035 _a(RuTPU)RU\TPU\network\615
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090 _a636585
100 _a20140217a2010 k y0engy50 ba
101 0 _aeng
102 _aUS
135 _adrnn ---uucaa
181 0 _ai
182 0 _ab
200 1 _aEfficient and economic halogenation of aryl amines via arenediazonium tosylate salts
_fYoung Min Lee [et al.]
203 _aText
_celectronic
300 _aTitle screen
320 _a[Referenses: p.7422 (29 tit.)]
330 _aArenediazonium tosylate salts have been successfully employed as a new and efficient reagent in halogenation reactions. A novel and economic protocol has been developed for the bromination and chlorination of various anilines using arenediazonium tosylate salts. A wide variety of reaction conditions were studied in acetonitrile at either room temperature or 60 °C in the presence or absence of catalyst with good to excellent yields. A surprising result showed the formation of acetanilides as a major product of aniline and methyl-substituted aniline halogenations in high yields
333 _aРежим доступа: по договору с организацией-держателем ресурса
461 _tTetrahedron Letters
_oScientific Journal
463 _tVol. 66, iss. 37
_v[P. 7418–7422]
_d2010
610 1 _aэлектронный ресурс
610 1 _aтруды учёных ТПУ
701 0 _aYoung Min Lee
701 0 _aMi Eun Moon
701 1 _aFilimonov
_bV. D.
_cRussian chemist
_cProfessor of the TPU
_f1945-
_gViktor Dmitrievich
_2stltpush
_3(RuTPU)RU\TPU\pers\26423
701 0 _aKi-Whan Chi
801 2 _aRU
_b63413507
_c20160419
_gRCR
856 4 _uhttp://www.sciencedirect.com/science/article/pii/S0040402010010446
942 _cCF