Artículos de revistas
Total syntheses of (R)-argentilactone and (R)-goniothalamin via catalytic enantioselective allylation of aldehydes
Registro en:
Tetrahedron Letters. Pergamon-elsevier Science Ltd, v. 44, n. 48, n. 8721, n. 8724, 2003.
0040-4039
WOS:000186474400021
10.1016/j.tetlet.2003.09.122
Autor
de Fatima, A
Pilli, RA
Institución
Resumen
The total syntheses of (R)-argentilactone (five steps, 25% overall yield) and (R)-goniothalamin (three steps, 61% overall yield) have been described through the enantioselective catalytic allylation of aldehydes (including a propargylic aldehyde) which provided a rapid access to these natural products that display very interesting biological activities. (C) 2003 Published by Elsevier Ltd. 44 48 8721 8724