Efficient and economic halogenation of aryl amines via arenediazonium tosylate salts; Tetrahedron Letters; Vol. 66, iss. 37

Efficient and economic halogenation of aryl amines via arenediazonium tosylate salts; Tetrahedron Letters; Vol. 66, iss. 37

Detalhes bibliográficos
Parent link:	Tetrahedron Letters: Scientific Journal Vol. 66, iss. 37.— 2010.— [P. 7418–7422]
Outros Autores:	Young Min Lee, Mi Eun Moon, Filimonov V. D. Viktor Dmitrievich, Ki-Whan Chi
Resumo:	Title screen Arenediazonium 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 Режим доступа: по договору с организацией-держателем ресурса
Idioma:	inglês
Publicado em:	2010
Assuntos:	электронный ресурс труды учёных ТПУ
Acesso em linha:	http://www.sciencedirect.com/science/article/pii/S0040402010010446
Formato:	Recurso Electrónico Capítulo de Livro
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=636585

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