Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
The carbonylation of ArLi (Ar = Ph, o-anisyl) in the presence of alkyl bromides affords diarylalkylcarbinols in good yields. The reaction may be used to obtain alcohols functionalized in the alkyl chain; it can also be adapted to afford substituted tetrahydrofurans. © 1981, American Chemical Society...
Guardado en:
| Publicado: |
1981
|
|---|---|
| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v46_n22_p4625_Nudelman http://hdl.handle.net/20.500.12110/paper_00223263_v46_n22_p4625_Nudelman |
| Aporte de: |
Ejemplares similares
-
Carbonylation of Aryllithium Reagents in the Presence of Alkyl Halides: One-Pot Synthesis of Diarylalkylcarbinols and Derivatives
por: Nudelman, N.S., et al. -
One-pot synthesis of diarylalkylcarbinols and substituted derivatives through carbon monoxide insertion reactions into aryllithiums
Publicado: (1987) -
One-pot synthesis of diarylalkylcarbinols and substituted derivatives through carbon monoxide insertion reactions into aryllithiums
por: Vitale, A.A., et al. -
Carbon-Carbon Bond Formation through the Carbonylation of Lithium Dialkylamides. One-Pot Synthesis of N-Alkyl-Substituted Formamides, Glyoxylamides, and Hydroxymalonamides
por: Perez, Daniel Gustavo
Publicado: (1988) -
Carbon-Carbon Bond Formation through the Carbonylation of Lithium Dialkylamides. One-Pot Synthesis of N-Alkyl-Substituted Formamides, Glyoxylamides, and Hydroxymalonamides
por: Pérez, D.G., et al.