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...
Hlavní autoři: | Hodgson, D, Kaka, N |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
John Wiley and Sons
2008
|
Podobné jednotky
-
Asymmetric synthesis of α-alkylated aldehydes using chiral enamines
Autor: Kaka, N, a další
Vydáno: (2008) -
Enantioenriched a-substituted aldehydes via diastereoselective enamine alkylation
Autor: Kaka, N, a další
Vydáno: (2007) -
Synthesis and C-alkylation of hindered aldehyde enamines.
Autor: Hodgson, D, a další
Vydáno: (2009) -
C-alkylation of chiral tropane- and homotropane-derived enamines.
Autor: Hodgson, D, a další
Vydáno: (2013) -
Enamines from terminal epoxides and hindered lithium amides.
Autor: Hodgson, D, a další
Vydáno: (2004)