15366-64-0Relevant academic research and scientific papers
A simple method for iodination of heterocyclic compounds using HIO 4/NaCl/silica gel/H2SO4 in water
Hosseini, Abolfazl,Khalilzadeh, Mohammad A.,Hosseinzadeh, Masoumeh,Tajbakhsh, Mahmoud
, p. 619 - 623 (2012)
A fast and simple method for iodination of some heterocycles is reported. The reactions were carried out in water, using HIO4/H 2SO4/NaCl/silica gel at moderate temperatures of 25-50 °C. Springer-Verlag 2011.
Cheap and easy synthesis of highly functionalized (het)aryl iodides via the aromatic finkelstein reaction
Meyer-Eppler, Georg,Kuechler, Lea,Tenten, Christina,Benkhaeuser, Christian,Brueck, Stefanie,Luetzen, Arne
, p. 1085 - 1090 (2014/05/06)
Aryl iodides are superior coupling partners in cross-couplingA- reactions compared to the corresponding chlorides or bromides. Unfortunately, the iodides are much more expensive, if commercially available at all, than the other halides. Thus, it is often mandatory to transform the available bromides into the corresponding iodides. The copper-catalyzed aromatic Finkelstein reaction turned out to be the method of choice to prepare a number of highly functionalized iodo(het)aryls, including pyridines, 2,2′-bipyridines, and chiral compounds. Georg Thieme Verlag Stuttgart? New York.
