A Green Procedure for the Diazotization-Iodination of Aromatic Amines under Aqueous, Strong-Acid-Free Conditions

Bibliographic Details
Parent link:	Journal of Synthetic Organic Chemistry. Synthesis: Scientific Journal 13.— 2011.— [P. 2154-2158]
Other Authors:	Trusova M. E. Marina Evgenievna, Krasnokutskaya E. A . Elena Aleksandrovna, Postnikov P. S. Pavel Sergeevich, Younghwa Choi, Ki-Whan Chi, Filimonov V. D. Viktor Dmitrievich
Summary:	Title screen A convenient and mild one-pot method for the synthesis of iodoarenes in high yields by the sequential diazotization-iodination of aromatic amines with a reusable polymeric diazotization agent in the presence of p-toluenesulfonic acid at room temperature in water was developed. The method is general and is the greenest alternative of the known diazotization-iodination methods. The method is also effective for the preparation of 1H-benzo[d][1,2,3]triazole and benzo[d][1,2,3]thiadiazole Режим доступа: по договору с организацией-держателем ресурса
Published:	2011
Subjects:	электронный ресурс труды учёных ТПУ диазотирование diazotization halogenation iodination иодирование гетероциклы heterocycles амины amines
Online Access:	https://www.thieme-connect.de/ejournals/html/10.1055/s-0030-1260046
Format:	Electronic Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=636574

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