@article { ISI:000372175300004,
	title = {I-2-mediated regioselective C-3 azidation of indoles},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {14},
	number = {11},
	year = {2016},
	month = {FEB},
	pages = {3027-3030},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>An unprecedented synthesis of novel 3-azido indoles has been developed using I-2 and NaN3 in high yields and excellent regio-selectivity. The reaction proceeds under metal-free conditions at room temperature. Essentially, an umpolung in reactivity at the C-3 position of indole has been achieved by the activation of indoles with I-2.</p>},
	issn = {1477-0520},
	doi = {10.1039/c6ob00295a},
	author = {Prasad, Pragati K. and Kalshetti, Rupali G. and Reddi, Rambabu N. and Kamble, Sanjay P. and Sudalai, Arumugam}
}
@article {46182,
	title = {Iridium(III)-catalyzed alkynylation of 2-(Hetero)arylquinazolin-4-one scaffolds via C-H bond activation},
	journal = {Journal of Organic Chemistry},
	volume = {84},
	year = {2019},
	month = {MAR },
	pages = {2951-2961},
	type = {Article},
	abstract = {<p>The directed C-H alkynylation of 2-(hetero)arylquinazolin-4-ones has been explored with the ethynylbenziodoxolone reagent TIPS-EBX employing an Ir(III) catalyst. Complementary conditions for either monoalkynylation or dialkynylation have been developed. Also demonstrated is the broad scope of this reaction and the compatibility of various functional groups such as -F, -Cl, -Br, -CF3, -OMe, -NO2, and alkyl, etc.</p>
},
	issn = {0022-3263},
	doi = {10.1021/acs.joc.8b02738},
	author = {Rohokale, Rajendra S. and Kalshetti, Rupali G. and Ramana, Chepuri V.}
}
