Artículos de revistas
A Concise Route To The Azaspirodecane Moiety Of Halichlorine And Structurally Related Alkaloids.
Registro en:
Organic Letters. v. 7, n. 8, p. 1617-9, 2005-Apr.
1523-7060
10.1021/ol050306g
15816766
Autor
de Sousa, Andrea L
Pilli, Ronaldo A
Institución
Resumen
[reaction: see text] A tandem Michael addition-enolate alkylation followed by Dieckmann cyclization and Beckmann rearrangement provided the corresponding [5.4.0] azaspirobicyclodecane, a key intermediate in our synthetic route to the marine alkaloid halichlorine (1). 7 1617-9