@article { ISI:000260397500006,
	title = {NaIO4-KI-NaN3 as a new reagent system for C-H functionalization in hydrocarbons},
	journal = {Tetrahedron Letters},
	volume = {49},
	number = {45},
	year = {2008},
	month = {NOV},
	pages = {6401-6403},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>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. (C) 2008 Elsevier Ltd. All rights reserved.</p>},
	keywords = {azides, C-H activation, Iodination, NaIO4},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2008.08.071},
	author = {Chouthaiwale, Pandurang V. and Suryavanshi, Gurunath and Sudalai, Arumugam}
}
@article { ISI:000284533700013,
	title = {Regiospecific azidoiodination of alkenes with sodium periodate, potassium iodide, and sodium azide: a high-yield synthesis of beta-iodoazides},
	journal = {Synthesis-Stuttgart},
	number = {22},
	year = {2010},
	month = {NOV},
	pages = {3879-3882},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The combination of sodium periodate, potassium iodide, and sodium azide has been found to be an efficient, simple, and inexpensive reagent system for azidoiodination of alkenes. The regiospecific 1,2-azidoiodination proceeds in an anti-Markovnikov fashion to produce beta-iodoazides in excellent yields.</p>},
	keywords = {alkenes, azides, azidoiodination, beta-iodoazides, regio-specific},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1258250},
	author = {Chouthaiwale, Pandurang V. and Karabal, Pratibha U. and Suryavanshi, Gurunath and Sudalai, Arumugam}
}
