@article { ISI:000344635200043,
	title = {I-2-catalyzed regioselective Oxo- and hydroxy-acyloxylation of alkenes and enol ethers: a facile access to alpha-acyloxyketones, esters, and diol derivatives},
	journal = {Organic Letters},
	volume = {16},
	number = {21},
	year = {2014},
	month = {NOV},
	pages = {5674-5677},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>I-2-catalyzed oxo-acyloxylation of alkenes and enol ethers with carboxylic acids providing for the high yield synthesis of a-acyloxyketones and esters is described. This unprecedented regioselective oxidative process employs TBHP and Et3N in stoichiometric amounts under metal-free conditions in DMSO as solvent. Additionally, I-2-catalysis allows the direct hydroxy-acyloxylation of alkenes with the sequential addition of BH3 center dot SMe2 leading to monoprotected diol derivatives in excellent yields.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol5027393},
	author = {Reddi, Rambabu N. and Prasad, Pragati K. and Sudalai, Arumugam}
}
@article { ISI:000372175300004,
	title = {I-2-mediated regioselective C-3 azidation of indoles},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {14},
	number = {11},
	year = {2016},
	month = {FEB},
	pages = {3027-3030},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>An unprecedented synthesis of novel 3-azido indoles has been developed using I-2 and NaN3 in high yields and excellent regio-selectivity. The reaction proceeds under metal-free conditions at room temperature. Essentially, an umpolung in reactivity at the C-3 position of indole has been achieved by the activation of indoles with I-2.</p>},
	issn = {1477-0520},
	doi = {10.1039/c6ob00295a},
	author = {Prasad, Pragati K. and Kalshetti, Rupali G. and Reddi, Rambabu N. and Kamble, Sanjay P. and Sudalai, Arumugam}
}
