Artículos de revistas
Synthesis of indole derivatives by domino hydroformylation/indolization of 2-nitrocinnamaldehydes
Fecha
2008Registro en:
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, v.288, n.1/Fev, p.103-108, 2008
1381-1169
10.1016/j.molcata.2008.03.025
Autor
MARCHETTI, M.
PAGANELLI, S.
CARBONI, D.
ULGHERI, F.
PONTE, G. Del
Institución
Resumen
The present work furnishes an innovative preparation of substituted indoles based on tandem hydroformylation, where the chemo- and the regio-selectivities are good, so the yield of the reaction. The novelty has been established in the four-step transformation of substituted alpha nitrocinnamaldehydes into desired indoles in a one-pot reaction. Under hydroformylation reaction conditions we have been able to trigger off a cascade of reactions, which gave substituted indoles in high yields. Useful intermediates are prepared by using this technique for the synthesis of well-known biologically active molecules. (C) 2008 Elsevier B.V. All rights reserved.