@article { ISI:000260210000002,
	title = {Thallium(III) p-tosylate mediated oxidative 2,3-aryl rearrangement: a new useful route to ipriflavone and its analogs},
	journal = {Synthetic Communications},
	volume = {38},
	number = {22},
	year = {2008},
	month = {MAR},
	pages = {3875-3883},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>A new route for the synthesis of ipriflavone, an antiosteoporotic agent, is described that has four steps and 60\% yields starting from resacetophenone (2). The key step of the present methodology is thallium(III) p-tosylate mediated oxidative 2,3-aryl rearrangement of flavanone to generate the isoflavone ring system of ipriflavone in a highly efficient manner.</p>},
	keywords = {Flavanones, ipriflavone, isoflavones, oxidative rearrangement, thallium(III) p-tosylate},
	issn = {0039-7911},
	doi = {10.1080/00397910802238734},
	author = {Muthukrishnan, Murugan and Singh, Om V.}
}
