@article {3663,
	title = {A remarkable multiple rearrangement process in the bromination of endo-3-bromo-4-methylcamphor: Intermediates for triterpenoid synthesis},
	journal = {Tetrahedron},
	volume = {52},
	number = {47},
	year = {1996},
	note = {ISI Document Delivery No.: VT272Times Cited: 2Cited Reference Count: 36},
	month = {Nov},
	pages = {14661-14672},
	type = {Article},
	abstract = {The remarkable transformation of endo-3-bromo-4-methylcamphor (9) to endo-3,9-dibromo-4-(bromomethyl)camphor (11) forms the basis of a new approach to intermediates for the synthesis of lanostane triterpenoids, euphane triterpenoids and 14 alpha-methyl steroids. Copyright (C) 1996 Elsevier Science Ltd},
	keywords = {4-METHYLCAMPHOR, CAMPHOR, CYCLIZATION, DERIVATIVES, ENANTIOSPECIFIC SYNTHESIS, NATURAL PRODUCT SYNTHESIS, ORGANIC-SYNTHESIS, ROUTE, STEROID-SYNTHESIS, SYNTHONS},
	isbn = {0040-4020},
	url = {<Go to ISI>://A1996VT27200003},
	author = {Ferguson, C. G. and Money, T. and Pontillo, J. and Whitelaw, P. D. M. and Wong, M. K. C.}
}
@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.}
}
