Asymmetric synthesis of alpha-alkylated aldehydes using terminal epoxide-derived chiral enamines.
(Chemical Equation Presented) Effective discrimination: Efficient lithium amide-induced terminal epoxide-enamine transformation provides the first enamines capable of generating α-alkylated aldehydes with high asymmetric induction by intermolecular nucleophilic substitution (see scheme). © 2008 Wile...
Autores principales: | Hodgson, D, Kaka, N |
---|---|
Formato: | Journal article |
Lenguaje: | English |
Publicado: |
John Wiley and Sons
2008
|
Ejemplares similares
-
Asymmetric synthesis of α-alkylated aldehydes using chiral enamines
por: Kaka, N, et al.
Publicado: (2008) -
Enantioenriched a-substituted aldehydes via diastereoselective enamine alkylation
por: Kaka, N, et al.
Publicado: (2007) -
Synthesis and C-alkylation of hindered aldehyde enamines.
por: Hodgson, D, et al.
Publicado: (2009) -
C-alkylation of chiral tropane- and homotropane-derived enamines.
por: Hodgson, D, et al.
Publicado: (2013) -
Enamines from terminal epoxides and hindered lithium amides.
por: Hodgson, D, et al.
Publicado: (2004)