@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.}
}
@article {7036,
	title = {STEREOSELECTIVITY OF C(3) METHYLATION AND ALDOL CONDENSATION OF CAMPHOR AND DERIVATIVES},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 14Cited Reference Count: 38},
	month = {Mar},
	pages = {558-566},
	type = {Article},
	abstract = {The stereoselectivity of methylation and aldol condensation of camphor and derivatives is determined by the presence or absence of a C(7) syn-methyl group and (or) C(5) and C(6) endo-hydrogen atoms.},
	keywords = {APPROACH, BICYCLO<2.2.1>HEPTANES, C(3)ALDOL, C(3)METHYLATION, CAMPHOR, NUCLEAR MAGNETIC-RESONANCE, ORGANIC-SYNTHESIS, PSEUDOGUAIANOLIDES, STEREOCONTROLLED, VITAMIN-D METABOLITES},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800029},
	author = {Hutchinson, J. H. and Li, D. L. F. and Money, T. and Palme, M. and Agharahimi, M. R. and Albizati, K. F.}
}
