@article { ISI:000340517200050,
	title = {Total synthesis of (+/-)-nardoaristolone B and its analogues},
	journal = {Organic Letters},
	volume = {16},
	number = {16},
	year = {2014},
	month = {AUG},
	pages = {4252-4255},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The first total synthesis of nardoaristolone B, a nor-sesquiterpenoid with an unusual fused ring system and having protective effects on the injury of neonatal rat cardiomyocytes, has been accomplished. Stereoselective synthesis of its novel analogues inlcuding exo-cyclopropyl ring fusion is also part of this disclosure. In addition, an alternate and more efficient one-step method to make a 3/5/6 tricyclic ring system using the Robinson annulation method has been developed toward the generation of a library of compounds around this skeleton.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol501949r},
	author = {Handore, Kishor L. and Reddy, D. Srinivasa}
}
