@article {2530,
	title = {Oxidation of Oximes to Nitrile Oxides with Hypervalent Iodine Reagents},
	journal = {Organic Letters},
	volume = {11},
	number = {7},
	year = {2009},
	note = {ISI Document Delivery No.: 425FOTimes Cited: 21Cited Reference Count: 33Mendelsohn, Brian A. Lee, Shelley Kim, Simon Teyssier, Florian Aulakh, Virender S. Ciufolini, Marco A.},
	month = {Apr},
	pages = {1539-1542},
	type = {Article},
	abstract = {Iodobenzene diacetate in MeOH containing a catalytic amount of TFA efficiently oxidizes aldoximes to nitrile oxides. The latter may be trapped in situ with olefins in a bimolecular or an intramolecular mode. The new method enables the execution of tandem oxidative dearomatization of phenols/intramolecular nitrile oxide cycloaddition sequences leading to useful synthetic intermediates.},
	keywords = {AMIDATION, CARBONYL-COMPOUNDS, CHEMISTRY, CONVERSION, DESS-MARTIN PERIODINANE, DIRECTIONS, FR901483, PHENOLS, TOSYLATES, TOSYLHYDRAZONES},
	isbn = {1523-7060},
	url = {<Go to ISI>://000264622600020},
	author = {Mendelsohn, B. A. and Lee, S. and Kim, S. and Teyssier, F. and Aulakh, V. S. and Ciufolini,Marco A.}
}
@article {2159,
	title = {Improved procedure for the bimolecular oxidative amidation of phenols},
	journal = {Journal of Organic Chemistry},
	volume = {73},
	number = {11},
	year = {2008},
	note = {ISI Document Delivery No.: 307MRTimes Cited: 17Cited Reference Count: 24Liang, Huan Ciufolini, Marco A.},
	month = {Jun},
	pages = {4299-4301},
	type = {Article},
	abstract = {Trifluoroacetic acid (TFA) is an effective promoter of the bimolecular Ritter-like oxidative amidation of 4-substituted phenols induced by PhI(OAc)(2) in MeCN. This suppresses the need for fluoroalcohol cosolvents, increases the yields, and facilitates isolation/purification procedures.},
	keywords = {DERIVATIVES, ETHERS, FR901483, HYPERVALENT IODINE OXIDATION, lactones, REAGENTS, SPIROLEUCETTADINE},
	isbn = {0022-3263},
	url = {<Go to ISI>://000256323500050},
	author = {Liang, H. and Ciufolini,Marco A.}
}
@article {1070,
	title = {Nitrogenous educts through oxidative amidation of phenols: The bimolecular reaction},
	journal = {Organic Letters},
	volume = {7},
	number = {2},
	year = {2005},
	note = {ISI Document Delivery No.: 887UFTimes Cited: 34Cited Reference Count: 29},
	month = {Jan},
	pages = {175-177},
	type = {Article},
	abstract = {The elusive oxidative amidation of phenols to 4-aza-substituted dienones in the bimolecular mode may be achieved by treatment with iodobenzene diacetate ("DIB") in a mixture of hexafluoro-2-propanol and acetonitrile.},
	keywords = {(-)-TAN1251A, AMIDES, AMINATION, ARENES, CYCLIZATION, DERIVATIVES, FR901483, HYPERVALENT IODINE OXIDATION, N-ACYLNITRENIUM IONS, TYROSINE},
	isbn = {1523-7060},
	url = {<Go to ISI>://000226330300003},
	author = {Canesi, S. and Bouchu, D. and Ciufolini,Marco A.}
}
