Artículos de revistas
A concise route to the azaspirodecane moiety of halichlorine and structurally related alkaloids
Registro en:
Organic Letters. Amer Chemical Soc, v. 7, n. 8, n. 1617, n. 1619, 2005.
1523-7060
WOS:000228344200046
10.1021/ol050306g
Autor
de Sousa, AL
Pilli, RA
Institución
Resumen
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 8 1617 1619