Ligand-Enabled Stereoselective ß-C(sp(3))-H Fluorination: Synthesis of Unnatural Enantiopure anti-ß-Fluoro-α-amino Acids.
J Am Chem Soc
; 137(22): 7067-70, 2015 Jun 10.
Article
em En
| MEDLINE
| ID: mdl-26001406
ABSTRACT
A quinoline-based ligand was shown to promote palladium-catalyzed ß-C(sp(3))-H fluorination for the first time. A range of unnatural enantiopure fluorinated α-amino acids were obtained through sequential ß-C(sp(3))-H arylation and subsequent stereoselective fluorination from readily available L-alanine.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Flúor
/
Aminoácidos
Idioma:
En
Revista:
J Am Chem Soc
Ano de publicação:
2015
Tipo de documento:
Article
País de afiliação:
Estados Unidos