@article {3768,
	title = {A formal, enantiospecific synthesis of pseudoguaianolides},
	journal = {Tetrahedron},
	volume = {52},
	number = {18},
	year = {1996},
	note = {ISI Document Delivery No.: UH378Times Cited: 16Cited Reference Count: 73},
	month = {Apr},
	pages = {6307-6324},
	type = {Article},
	abstract = {The preparation of ketal-enone (3) and hydroxy-ketones (1a), (16), and (4a), from (-)-camphor (6) represents a formal enantiospecific synthesis of (+)-carpesiolin, (+)-confertin, (-)-damsin, (-)-helenalin, (+)-bigelovin, (+)-mexicanin I, and (+)-linifolin A. Copyright (C) 1996 Elsevier Science Ltd},
	keywords = {(+)-CONFERTIN, (+/-)-CONFERTIN, ANTI-TUMOR LACTONES, CAMPHOR DERIVATIVES, DL-HELENALIN, inhibitors, ROUTE, SESQUITERPENE LACTONES, STEROID-SYNTHESIS, SYSTEM},
	isbn = {0040-4020},
	url = {<Go to ISI>://A1996UH37800004},
	author = {Money, T. and Wong, M. K. C.}
}
