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.
Asıl Yazarlar: | Bull, S, Davies, S, Delgado-Ballester, S, Fenton, G, Kelly, P, Smith, A |
---|---|
Materyal Türü: | Journal article |
Dil: | English |
Baskı/Yayın Bilgisi: |
2000
|
Benzer Materyaller
-
Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives
Yazar:: Bull, S, ve diğerleri
Baskı/Yayın Bilgisi: (2001) -
Asymmetric synthesis of beta-pyridyl-beta-amino acid derivatives
Yazar:: Bull, S, ve diğerleri
Baskı/Yayın Bilgisi: (2002) -
Asymmetric synthesis of beta-amino acid scaffolds
Yazar:: Bull, S, ve diğerleri
Baskı/Yayın Bilgisi: (2001) -
Asymmetric synthesis of beta-fluoroaryl-beta-amino acids
Yazar:: Davies, S, ve diğerleri
Baskı/Yayın Bilgisi: (2012) -
Asymmetric synthesis of homochiral differentially protected bis-beta-amino acid scaffolds
Yazar:: Bull, S, ve diğerleri
Baskı/Yayın Bilgisi: (2002)