@article {9805,
	title = {Synthetic aspects of the oxidative amidation of phenols.},
	journal = {Tetrahedron},
	volume = {66},
	year = {2010},
	note = {CAPLUS AN 2010:873196(Journal; General Review)},
	month = {2010///},
	pages = {5884 - 5892},
	publisher = {Elsevier Ltd.},
	abstract = {A review. The oxidative amidation of phenols effects the conversion of appropriately substituted phenols into 4-amidodienones (para-oxidative amidation{\textquoteright}) or 2-amidodienones (ortho-oxidative amidation{\textquoteright}) by the action of hypervalent iodine reagents. The reagent, (diacetoxyiodo)benzene (DIB{\textquoteright}) is esp. effective in these transformations. This paper focuses on techniques for the desymmetrization of the dienones thus obtained, leading to the stereocontrolled creation of N-substituted spiro carbons. The methodol. creates new opportunities in alkaloid synthesis, as apparent from a no. of examples. [on SciFinder(R)]},
	keywords = {review oxidative amidation phenol},
	isbn = {0040-4020},
	author = {Liang,Huan and Ciufolini,Marco A.}
}
