1.
Org Lett
; 2(3): 381-3, 2000 Feb 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-10814328
RESUMO
[reaction: see text] Angularly substituted, optically active bicyclic ketones of up to 94% ee were prepared by the Ti(II) alkoxide-mediated tandem cyclization of open-chain substrates, that is, 8-phenylmenthyl enynoates having a trisubstituted double bond.