@article { ISI:000249893900002,
	title = {NaIO4/LiBr-Mediated direct conversion of benzylic alcohols and aromatic aldehydes to aromatic esters},
	journal = {Synthetic Communications},
	volume = {37},
	number = {16},
	year = {2007},
	month = {AUG},
	pages = {2641-2646},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>Aromatic aldehydes or benzylic alcohols are directly converted to the corresponding aromatic esters in high yields on treatment with methanol or ethanol mediated by sodium metaperiodate (NaIO4)/LiBr in an acidic medium.</p>},
	keywords = {aromatic ester, benazaldehyde, Benzyl alcohol, Lithium bromide, Sodium metaperiodate},
	issn = {0039-7911},
	doi = {10.1080/00397910701465032},
	author = {Shaikh, Tanveer Mohammad Ali and Emmanuvel, Lourdusamy and Sudalai, Arumugam}
}
@article { ISI:000284664500025,
	title = {NaIO4/LiBr-mediated aziridination of olefins using chloramine-T},
	journal = {Tetrahedron Letters},
	volume = {51},
	number = {49},
	year = {2010},
	month = {DEC},
	pages = {6460-6462},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A new milder protocol for aziridination of a variety of olefins has been described. The process employs catalytic amount of sodium metaperiodate (NaIO4) as an oxidant and LiBr and chloramine-T as the bromine and nitrogen sources, respectively. Interestingly, the formation of aziridine products in all the cases studied takes place presumably through a process of 1,2-aminobromination of alkenes. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Aziridination, Chloramine-T, Lithium bromide, Olefin, Sodium metaperiodate},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2010.10.005},
	author = {Karabal, Pratibha U. and Chouthaiwale, Pandurang V. and Shaikh, Tanveer M. and Suryavanshi, Gurunath and Sudalai, Arumugam}
}
