@article { ISI:000372664600061,
	title = {Total synthesis of integrastatin B enabled by a benzofuran oxidative dearomatization cascade},
	journal = {Organic Letters},
	volume = {18},
	number = {6},
	year = {2016},
	month = {MAR},
	pages = {1458-1461},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The first total synthesis of integrastatin B, a potent HIV-1 integrase inhibitor, has been accomplished in seven steps with a 17.9\% overall yield employing easily accessible starting compounds. The Oxone-mediated oxidative benzofuran dearomatization cascade has been employed as the key skeletal construct to forge the central tetracyclic nucleus.</p>},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.6b00404},
	author = {More, Atul A. and Ramana, Chepuri V.}
}
