A one-pot process for the enantioselective synthesis of amines via reductive amination under transfer hydrogenation conditions.
Org Lett
; 5(22): 4227-30, 2003 Oct 30.
Article
em En
| MEDLINE
| ID: mdl-14572291
[reaction: see text]. Cyclic amines may be prepared via a sequence of deprotection followed by intramolecular reductive amination of t-Boc-protected amino ketones under asymmetric transfer hydrogenation conditions. In cases where the corresponding imine reaction proceeds with high enantioselectivity, this is reflected in the one-step process.
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Base de dados:
MEDLINE
Idioma:
En
Ano de publicação:
2003
Tipo de documento:
Article