@article { ISI:000292479300036,
	title = {Total synthesis of isofregenedadiol},
	journal = {Organic Letters},
	volume = {13},
	number = {14},
	year = {2011},
	month = {JUL},
	pages = {3690-3693},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The first total synthesis of isofregenedadiol, a bicyclic diterpene isolated from H. Viscosum, is reported starting from a D-(-)-pantolactone chiral pool. A one-pot quadruple reaction sequence comprising an enyne ring-closing metathesis/cross-metathesis/Diels-Alder/aromatization for the construction of a target skeleton Is the highlight of the present synthesis.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol201336x},
	author = {Kurhade, Suresh E. and Sanchawala, Abbas I. and Ravikumar, Velayutham and Bhuniya, Debnath and Reddy, D. Srinivasa}
}
