Investigation of preparative possibilities of iodinating systems on the basis of N-iodoacetamide

Bibliographic Details
Parent link:Bulletin of the Tomsk Polytechnic University/ Tomsk Polytechnic University (TPU).— , 2006-2007
Vol. 311, № 3.— 2007.— [P. 88-90]
Other Authors: Chaikovskii V. K. Vitold Kazimirovich, Funk A. A., Martynyuk O. A. Oksana Anatolievna, Kets T. S., Filimonov V. D. Viktor Dmitrievich
Summary:Заглавие с титульного листа
Электронная версия печатной публикации
N-iodoacetamide in organic solvents with H2SО4 iodinates successfully alkylbenzenes, aromatic amines and phenol ether. Electrophilic iodine activity is controlled by medium acidity. Super electrophilic iodine formed at N-iodoacetamide dissolution in sulfuric acid reacts easily with electron-deficient arenes at 0...20 °C forming iodinated products
Published: 2007
Series:Chemistry
Subjects:
Online Access:http://www.lib.tpu.ru/fulltext/v/Bulletin_TPU/2007/v311eng/i3/23.pdf
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=183005