@article {3767,
	title = {An enantiospecific synthetic approach to the limonoids},
	journal = {Chemical Communications},
	number = {5},
	year = {1996},
	note = {ISI Document Delivery No.: UG040Times Cited: 0Cited Reference Count: 30},
	month = {Mar},
	pages = {667-668},
	type = {Article},
	abstract = {Enone-ester 5, derived from (-)-9,10-dibromocamphor 3, is converted to a tricyclic enone 11 that may be of value in an enantiospecific synthesis of the limonoids.},
	keywords = {CAMPHOR DERIVATIVES, STEROID-SYNTHESIS, SYNTHONS, SYSTEM},
	isbn = {1359-7345},
	url = {<Go to ISI>://A1996UG04000046},
	author = {Money, T. and Richardson, S. R. and Wong, M. K. C.}
}
@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.}
}
@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 {2874,
	title = {AN ENANTIOSPECIFIC SYNTHESIS OF 4-METHYLCAMPHOR},
	journal = {Tetrahedron-Asymmetry},
	volume = {4},
	number = {11},
	year = {1993},
	note = {ISI Document Delivery No.: MJ468Times Cited: 10Cited Reference Count: 38},
	month = {Nov},
	pages = {2363-2370},
	type = {Article},
	abstract = {Treatment of (-)-2-methylenebornane (7), derived from (+)-camphor (1), with 45\% HBr /HOAc results in Wagner-Meerwein rearrangement and formation of 4-methylisobornyl bromide (17) in 80-90\% yield. The enantiopurity of (17) was determined by conversion to (+)-4-methylisoborneol (5) and (-)-4-methylcamphor (3).},
	keywords = {CAMPHOR DERIVATIVES, ESTERS, KETONES, NATURAL PRODUCT SYNTHESIS, POTASSIUM, REARRANGEMENTS, ROUTE, STEROID-SYNTHESIS, SYNTHONS},
	isbn = {0957-4166},
	url = {<Go to ISI>://A1993MJ46800024},
	author = {Money, T. and Palme, M. H.}
}
