7191-55-1Relevant articles and documents
Efficient and sustainable laccase-catalyzed iodination of: P -substituted phenols using KI as iodine source and aerial O2 as oxidant
Sdahl, Mark,Conrad, Jürgen,Braunberger, Christina,Beifuss, Uwe
, p. 19549 - 19559 (2019/07/05)
The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mild reaction conditions.
Ultrasound-promoted rapid and efficient iodination of aromatic and heteroaromatic compounds in the presence of iodine and hydrogen peroxide in water
Ferreira, Irlon M.,Casagrande, Gleison A.,Pizzuti, Lucas,Raminelli, Cristiano
supporting information, p. 2094 - 2102 (2014/07/07)
A rapid and efficient ultrasound-promoted protocol for iodination of aromatic and heteroaromatic compounds, using molecular iodine in the presence of aqueous hydrogen peroxide in water without any cosolvent, has produced versatile iodinated organic molecules with potential application in organic synthesis and medicine in short reaction times and good to excellent yields. Copyright
Efficient and selective iodination of phenols promoted by iodine and hydrogen peroxide in water
Gallo, Rafael D.C.,Gebara, Karimi S.,Muzzi, Rozanna M.,Raminelli, Cristiano
experimental part, p. 770 - 774 (2010/08/13)
A simple and selective reaction for the preparation of iodinated phenols was developed and phenol derivatives containing electron withdrawing groups were iodinated in very good yields under relatively mild conditions.
