A new, environment friendly protocol for iodination of electron-rich aromatic compounds
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Mild and regiospecific nuclear iodination of methoxybenzenes and naphthalenes with N-iodosuccinimide in acetonitrile
2. Synthetic methods and reactions. 181. Iodination of deactivated aromatics with N-iodosuccinimide in trifluoromethanesulfonic acid (NIS-CF3SO3H) via in situ generated superelectrophilic iodine(I) trifluoromethanesulfonate
3. Mild and regioselective iodination of electron-rich aromatics with N -iodosuccinimide and catalytic trifluoroacetic acid
4. A practical iodination of aromatic compounds using tetrabutylammonium peroxydisulfate and iodine
5. An Efficient and Regioselective Direct Aromatic Iodination Using Iodine and Nitrogen Dioxide
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