@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}
}
