@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 = {://A1996UH37800004}, author = {Money, T. and Wong, M. K. C.} }