@article { ISI:000338296300009,
	title = {2-Aroylindoles from o-bromochalcones via Cu(I)-catalyzed SNAr with an azide and intramolecular nitrene C-H insertion},
	journal = {Chemical Communications},
	volume = {50},
	number = {58},
	year = {2014},
	month = {May},
	pages = {7790-7792},
	publisher = {ROYAL SOC CHEMISTRY},
	type = {Article},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A simple procedure for the synthesis of 2-aroylindole derivatives comprising a one-pot CuI-catalyzed SNAr reaction of o-bromochalconeswith sodium azide and subsequent intramolecular cyclization through nitrene C-H insertion has been developed. This protocol is also applicablewith the 2{\textquoteright}-bromocinnamates giving the indole-2-carboxylates.</p>},
	issn = {1359-7345},
	doi = {10.1039/c4cc02501f},
	author = {Goriya, Yogesh and Ramana, Chepuri V.}
}
