@article { ISI:000322853000052,
	title = {Aryne insertion reactions leading to bioactive fused quinazolinones: diastereoselective total synthesis of cruciferane},
	journal = {Organic Letters},
	volume = {15},
	number = {15},
	year = {2013},
	month = {AUG},
	pages = {4006-4009},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>Insertion reactions of an in situ generated arynes to a variety of suitably substituted 1,3-quinazolin-4-ones have been demonstrated for a new efficient one-step approach to a diverse range of fused quinazolinone architectures. The present protocol has been effectively utilized to accomplish the concise total synthesis of recently isolated bioactive natural products tryptanthrin, phaitanthrins A-C, and cruciferane.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol4018062},
	author = {Vaidya, Sagar D. and N. P. Argade}
}
