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.
Үндсэн зохиолчид: | Bull, S, Davies, S, Delgado-Ballester, S, Fenton, G, Kelly, P, Smith, A |
---|---|
Формат: | Journal article |
Хэл сонгох: | English |
Хэвлэсэн: |
2000
|
Ижил төстэй зүйлс
-
Asymmetric synthesis of beta-haloaryl beta-amino acid derivatives
-н: Bull, S, зэрэг
Хэвлэсэн: (2001) -
Asymmetric synthesis of beta-pyridyl-beta-amino acid derivatives
-н: Bull, S, зэрэг
Хэвлэсэн: (2002) -
Asymmetric synthesis of beta-amino acid scaffolds
-н: Bull, S, зэрэг
Хэвлэсэн: (2001) -
Asymmetric synthesis of beta-fluoroaryl-beta-amino acids
-н: Davies, S, зэрэг
Хэвлэсэн: (2012) -
Asymmetric synthesis of homochiral differentially protected bis-beta-amino acid scaffolds
-н: Bull, S, зэрэг
Хэвлэсэн: (2002)