637-97-8Relevant articles and documents
NaIO4-KI-NaN3 as a new reagent system for C-H functionalization in hydrocarbons
Chouthaiwale, Pandurang V.,Suryavanshi, Gurunath,Sudalai, Arumugam
scheme or table, p. 6401 - 6403 (2009/04/06)
The NaIO4-KI-NaN3 combination has been found to be an efficient, reliable, and inexpensive reagent system for mono- and 1,2-difunctionalization of hydrocarbons via C-H bond activation to afford vicinal azido- and acetoxy iodinations of cyclic hydrocarbons.
New iodination reactions of saturated hydrocarbons
Barluenga, Jose,Campos-Gomez, Esther,Rodriguez, David,Gonzalez-Bobes, Francisco,Gonzalez, Jose M.
, p. 5851 - 5854 (2007/10/03)
Unactivated C-H bonds react with iodine when exposed to trimethylsilyl azide in the presence of a hypervalent iodine reagent or, alternatively, to aqueous H2O2, acetic anhydride, and sodium azide (see scheme). (Chemical Equation Presented).
Direct Iodination of Alkanes
Montoro, Raul,Wirth, Thomas
, p. 4729 - 4731 (2007/10/03)
(Matrix presented) A cheap and efficient iodination of hydrocarbons can be achieved by generating tert-butyl hypoiodite from iodine and sodium tert-butoxide. The alkane is reactant and solvent, and this metal-free process provides a clean solution for their direct iodination.