The asymmetric synthesis of beta-haloaryl-beta-amino acid derivatives
Lithium N-benzyl-N-α-methyl-4-methoxybenzylamide is employed as a homochiral ammonia equivalent for the asymmetric synthesis of β-haloaryl-β-amino acid derivatives using a conjugate addition/oxidative deprotection strategy.
Main Authors: | Bull, S, Davies, S, Delgado-Ballester, S, Fenton, G, Kelly, P, Smith, A |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado em: |
2000
|
Registos relacionados
-
Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives
Por: Bull, S, et al.
Publicado em: (2001) -
Asymmetric synthesis of beta-pyridyl-beta-amino acid derivatives
Por: Bull, S, et al.
Publicado em: (2002) -
Asymmetric synthesis of beta-amino acid scaffolds
Por: Bull, S, et al.
Publicado em: (2001) -
Asymmetric synthesis of beta-fluoroaryl-beta-amino acids
Por: Davies, S, et al.
Publicado em: (2012) -
Asymmetric synthesis of homochiral differentially protected bis-beta-amino acid scaffolds
Por: Bull, S, et al.
Publicado em: (2002)