@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 = {://A1992JL87000031}, author = {Clase, J. A. and Money, T.} }