One-pot biocatalyzed preparation of substituted amides as intermediates of pharmaceuticals
A lipase-catalyzed procedure is described for the one-pot conversion of carboxylic acids into substituted amides via in-situ formation of the ethyl ester and subsequent aminolysis. The procedure was optimized for the preparation of tetrahydro-N-[3-(methylamino)-propyl]-2-furancarboxamide, an interme...
Guardado en:
| Autores principales: | Baldessari, Alicia, Mangone, Constanza Pía |
|---|---|
| Publicado: |
2001
|
| Materias: | |
| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13811177_v11_n4-6_p335_Baldessari http://hdl.handle.net/20.500.12110/paper_13811177_v11_n4-6_p335_Baldessari |
| Aporte de: |
Ejemplares similares
-
One-pot biocatalyzed preparation of substituted amides as intermediates of pharmaceuticals
por: Baldessari, A., et al. -
Lipases as catalysts in synthesis of fine chemicals
por: Baldessari, A. -
Lipases as catalysts in synthesis of fine chemicals
Publicado: (2012) -
Enzyme-catalyzed preparation of chenodeoxycholic esters by an immobilized heterologous Rhizopus oryzae lipase
por: Quintana, Paula Gabriela, et al.
Publicado: (2015) -
Chemo-enzymatic synthesis of 1-O-hexadecyl-2-O-palmitoyl-sn-glycerol
por: Salto, María Laura, et al.
Publicado: (1997)