@article { ISI:000265962600005,
	title = {Cu(I)-promoted one-pot {\textquoteleft}SNAr-click reaction{\textquoteright} of fluoronitrobenzenes},
	journal = {Tetrahedron},
	volume = {65},
	number = {20},
	year = {2009},
	month = {MAY},
	pages = {3974-3979},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A one-pot two-step sequence involving a nucleophilic aromatic substitution (SNAF) of activated fluorobenzenes with azide nucleophile and in situ Huisgen cycloaddition of the resulting aryl azides with alkynes has been developed for a rapid access to 1,4-substituted triazoles. Control experiments revealed that both the steps are catalyzed by Cu(I) and also the course of reaction as SNAr followed by [3+2]-cycloaddition. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2009.03.035},
	author = {Durugkar, Kulbhushan A. and Gonnade, Rajesh G. and Ramana, C. V.}
}
