Kinetic Resolution of Benzylamines via Palladium(II)-Catalyzed C-H Cross-Coupling.
J Am Chem Soc
; 138(24): 7796-800, 2016 06 22.
Article
em En
| MEDLINE
| ID: mdl-27249208
ABSTRACT
A Pd(II)-catalyzed enantioselective C-H cross-coupling of benzylamines via kinetic resolution has been achieved using chiral mono-N-protected α-amino-O-methylhydroxamic acid (MPAHA) ligands. Both chiral benzylamines and ortho-arylated benzylamines are obtained in high enantiomeric purity. The use of a readily removable nosyl (Ns) protected amino group as the directing group is a crucial practical advantage. Moreover, the ortho-arylated benzylamine products could be further transformed into chiral 6-substituted 5,6-dihydrophenanthridines as important structural motifs in natural products and bioactive molecules.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Paládio
/
Benzilaminas
/
Reagentes de Ligações Cruzadas
Idioma:
En
Ano de publicação:
2016
Tipo de documento:
Article