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

Citation
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
Citations number
18
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
5
Year of publication
1999
Pages
907 - 910
Database
ISI
SICI code
0040-4039(19990129)40:5<907:ANSFTE>2.0.ZU;2-C
Abstract
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.