@article { ISI:000356054600003,
	title = {Oxidant controlled regio- and stereodivergent azidohydroxylation of alkenes via I-2 catalysis},
	journal = {Chemical Communications},
	volume = {51},
	number = {51},
	year = {2015},
	month = {APR},
	pages = {10276-10279},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A novel, I-2 catalyzed regio-and stereodivergent vicinal azidohydroxylation of alkenes leading to 1,2-azidoalcohols in high yields (up to 92\%) and excellent dr (up to 98\%) has been developed. This unprecedented transformation employs NaN3 and DMF as N-and O-nucleophiles respectively. The role of DMF as the O-source in the reaction has been unequivocally proven by O-18 labelling studies.</p>},
	issn = {1359-7345},
	doi = {10.1039/c5cc02374b},
	author = {Prasad, P. K. and Reddi, R. N. and Sudalai, A.}
}
