Mild and efficient synthesis of iodylarenes using Oxone as oxidant

Bibliographic Details
Parent link:	Tetrahedron Letters Vol. 57, iss. 37.— 2016.— [P. 4254-4256]
Corporate Author:	Национальный исследовательский Томский политехнический университет Институт природных ресурсов Кафедра технологии органических веществ и полимерных материалов
Other Authors:	Soldatova N. S. Nataliya Sergeevna, Postnikov P. S. Pavel Sergeevich, Troyan A. A. Anna Alekseevna, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Zhdankin V. V. Viktor Vladimirovich, Yoshimura A. Akira
Summary:	Title screen Mild and efficient method for the preparation of iodylarenes by oxidation of iodoarenes with Oxone in aqueous acetonitrile at room temperature is described. This new procedure allows the preparation of various iodylarenes with electron-donating or electron-withdrawing substituents in the aromatic ring including the previously unknown 1,2-diiodylbenzene. Режим доступа: по договору с организацией-держателем ресурса
Published:	2016
Subjects:	электронный ресурс труды учёных ТПУ йод окисление гипервалентные связи
Online Access:	http://dx.doi.org/10.1016/j.tetlet.2016.08.038
Format:	Electronic Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=650301

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