@article {2589,
	title = {Synthetic Studies toward Sordarin: Building Blocks for the Terpenoid Core and for Analogues Thereof},
	journal = {Journal of Organic Chemistry},
	volume = {74},
	number = {4},
	year = {2009},
	note = {ISI Document Delivery No.: 406TATimes Cited: 2Cited Reference Count: 73Schule, Arnaud Liang, Huan Vors, Jean-Pierre Ciufolini, Marco A.},
	month = {Feb},
	pages = {1587-1597},
	type = {Article},
	abstract = {Avenues to bi- and tricyclic building blocks for the elaboration of sordaricin and its analogues are described. The target molecules were obtained through inter- and intramolecular Diels-Alder reactions of a number of previously unknown cyclopentadienes. Unusual properties of 3-cyanoenones and 1-cyanocyclopentadienes have been unveiled and circumvented.},
	keywords = {ANTIFUNGAL SORDARINS, BAYLIS-HILLMAN REACTION, DERIVATIVES, ELONGATION-FACTOR 2, ENOLATE FORMATION, FUNGAL PROTEIN-SYNTHESIS, KETONE ENOLIZATION, LITHIUM DIALKYLAMIDES, RING-CLOSURE, SODIUM-BOROHYDRIDE},
	isbn = {0022-3263},
	url = {<Go to ISI>://000263316600020},
	author = {Schule, A. and Liang, H. and Vors, J. P. and Ciufolini,Marco A.}
}
