@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 {1369,
	title = {Synthetic ventures inspired by biosynthetic hypotheses: the evolution of a method for the oxidative amidation of phenols},
	journal = {Tetrahedron},
	volume = {62},
	number = {22},
	year = {2006},
	note = {ISI Document Delivery No.: 045ONTimes Cited: 22Cited Reference Count: 141Ciufolini, Marco A. Canesi, Sylvain Ousmer, Malika Braun, Norbert A.},
	month = {May},
	pages = {5318-5337},
	type = {Review},
	abstract = {We describe the development of a technique for the oxidative conversion of 4-alkyl phenols to derivatives of the corresponding 4-alkyl-4-amino-2,5-cyclohexanediones. This transformation, which was inspired by biogenetic considerations, constitutes a key step in the total syntheses of FR-901483, TAN-1251C, and cylindricine C. (c) 2006 Elsevier Ltd. All rights reserved.},
	keywords = {ALPHA-AMINO-ALDEHYDES, AROMATIC-SUBSTITUTION, ASCIDIAN CLAVELINA-CYLINDRICA, ELECTROPHILIC, HIGH ENANTIOMERIC EXCESS, HYPERVALENT IODINE OXIDATION, IMMUNOSUPPRESSANT FR901483, MANNICH CYCLIZATION APPROACH, MARINE ALKALOIDS, N-ACYLNITRENIUM IONS, NITROGEN HETEROCYCLIC-COMPOUNDS, POTENT, TRICYCLIC},
	isbn = {0040-4020},
	url = {<Go to ISI>://000237751500016},
	author = {Ciufolini,Marco A. and Canesi, S. and Ousmer, M. and Braun, N. 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.}
}
