@article { ISI:000364435000072,
	title = {Synthesis of N-aryl beta-amino alcohols by trifluoroacetic acid promoted multicomponent coupling of aziridines, arynes, and water},
	journal = {Journal of Organic Chemistry},
	volume = {80},
	number = {21},
	year = {2015},
	month = {NOV},
	pages = {11131-11137},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A transition-metal-free, three-component coupling involving N-substituted aziridines, arynes, and water promoted by trifluoroacetic acid (TFA) has been reported. The reaction furnished medicinally important N-aryl beta-amino alcohol derivatives in moderate to good yields. In addition, the use of azetidines in this reaction afforded N-aryl gamma-amino alcohol derivatives.</p>},
	issn = {0022-3263},
	doi = {10.1021/acs.joc.5b01798},
	author = {Roy, Tony and Baviskar, Dnyaneshwar R. and Biju, Akkattu T.}
}
@article { ISI:000366878300084,
	title = {Three-component coupling involving arynes, aromatic tertiary amines, and aldehydes via aryl-aryl amino group migration},
	journal = {Organic Letters},
	volume = {17},
	number = {24},
	year = {2015},
	month = {DEC},
	pages = {6270-6273},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The transition-Metal-free multicomponent coupling of arynes, aromatic tertiary amines, and aldehydes proceeding via the aryl to aryl amino group migration has been demonstrated. This protocol allows rapid access to ortho-functionalized tertiary amines in moderate to good yields. Moreover, activated ketones can also be used as the aldehyde Component in the present reaction. The similarity of the aryl-aryl tertiary amino group migration with the Smiles rearrangement is striking.</p>},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.5b03319},
	author = {Bhojgude, Sachin Suresh and Baviskar, Dnyaneshwar R. and Gonnade, Rajesh G. and Biju, Akkattu T.}
}
