@article {1615,
	title = {Studies toward soraphen A: An aldol-metathesis avenue to the macrocyclic framework},
	journal = {Organic Letters},
	volume = {8},
	number = {13},
	year = {2006},
	note = {ISI Document Delivery No.: 053DITimes Cited: 5Cited Reference Count: 63Vincent, Guillaume Mansfield, Darren J. Vors, Jean-Pierre Ciufolini, Marco A.},
	month = {Jun},
	pages = {2791-2794},
	type = {Article},
	abstract = {We describe a convergent approach to soraphen A, 1, that involves coupling of two fragments by an aldol condensation - olefin metathesis sequence. This route permits rapid access to congeners of 1.},
	keywords = {ALPHA-HYDROXYALLYLATION, ANTIFUNGAL, CARBONYL-COMPOUNDS, CHIRAL ALDEHYDES, ENANTIOSELECTIVE SYNTHESIS, GLIDING BACTERIA, MACROLIDE, OLEFIN METATHESIS, ORGANIC-SYNTHESIS, SILYL ETHERS, STEREOSELECTIVE SYNTHESIS},
	isbn = {1523-7060},
	url = {<Go to ISI>://000238284500034},
	author = {Vincent, G. and Mansfield, D. J. and Vors, J. P. and Ciufolini,Marco A.}
}
@article {7201,
	title = {AN ENANTIOSPECIFIC ROUTE TO C,D RING SYNTHONS FOR STEROID-SYNTHESIS},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {70},
	number = {5},
	year = {1992},
	note = {ISI Document Delivery No.: JL870Times Cited: 18Cited Reference Count: 68},
	month = {May},
	pages = {1537-1544},
	type = {Article},
	abstract = {A simple enantiospecific route to a hydrindenone intermediate for steroid synthesis has been accomplished. The introduction of a wide variety of side-chain units is made possible hy stereoselective alkylation of a bicyclic ester 13 derived from (+)-camphor 4.},
	keywords = {APPROACH, asymmetric, CONSTRUCTION, Diels-Alder, ENANTIOSELECTIVE SYNTHESIS, GAMMA-BUTYROLACTONE DERIVATIVES, INHOFFEN-LYTHGOE DIOL, SIDE-CHAIN CONSTRUCTION, STEREOCONTROLLED, STEREOSELECTIVE SYNTHESIS, TANDEM ALKYLATION, TRIPLY CONVERGENT SYNTHESIS, VITAMIN-D METABOLITES},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1992JL87000031},
	author = {Clase, J. A. and Money, T.}
}
