A novel strategy for the enantioselective synthesis of the steroidal framework using cascade ring expansion reactions of small ring systems - Asymmetric total synthesis of (+)-equilenin
H. Nemoto et al., A novel strategy for the enantioselective synthesis of the steroidal framework using cascade ring expansion reactions of small ring systems - Asymmetric total synthesis of (+)-equilenin, TETRAHEDR L, 40(5), 1999, pp. 907-910
Enantioselective synthesis of (+)-equilenin (1) utilizing a novel strategy
is described. The key steps are two cascade ring expansion reactions of sma
ll ring systems; 1) chiral (salen)Mn-III complex-catalyzed cascade reaction
of cyclopropylidene; 2) Pd-II-mediated cascade reaction of the cyclobutano
l. (C) 1999 Elsevier Science Ltd. All rights reserved.