309757-67-3Relevant academic research and scientific papers
Asymmetric synthesis of β-haloaryl β-amino acid derivatives
Bull, Steven D.,Davies, Stephen G.,Delgado-Ballester, Santiago,Kelly, Peter M.,Kotchie, Luke J.,Gianotti, Massimo,Laderas, Mario,Smith, Andrew D.
, p. 3112 - 3121 (2007/10/03)
Lithium N-benzyl-N-α-methyl-4-methoxybenzylamide may be employed as a homochiral ammonia equivalent for the synthesis of homochiral β-haloaryl β-amino acid derivatives via a strategy involving its conjugate addition to α,β-unsaturated β-haloaryl acceptors and subsequent oxidative deprotection with ceric ammonium nitrate.
The asymmetric synthesis of β-haloaryl-β-amino acid derivatives
Bull,Davies,Delgado-Ballester,Fenton,Kelly,Smith
, p. 1257 - 1260 (2007/10/03)
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.
