@article { ISI:000378390300022,
	title = {Efficient access to alkynylated quinalizinones via the gold(I)-catalyzed aminoalkynylation of alkynes},
	journal = {Chemical Communications},
	volume = {52},
	number = {52},
	year = {2016},
	month = {MAY},
	pages = {8152-8155},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>The gold-catalyzed aminoalkynylation of alkynes for the synthesis of quinalizinones is reported. For instance, the reaction of pyridinoalkynes with 1-[(triisopropylsilyl)-ethynyl]-1,2-benziodoxol-3(1H)-one (TIPS-EBX) in the presence of a catalytic amount of AuCl at 50 8C afforded alkynylated quinalizinones in 57-87\% yields.</p>},
	issn = {1359-7345},
	doi = {10.1039/c6cc03414d},
	author = {Shinde, Popat S. and Shaikh, Aslam C. and Patil, Nitin T.}
}
