134420-70-5Relevant articles and documents
Improved enzymatic syntheses of valuable β-arylalkyl-β-amino acid enantiomers
Tasnadi, Gabor,Forro, Enik,Fueloep, Ferenc
experimental part, p. 793 - 799 (2010/06/20)
The enantioselective (E~ 200) Burkholderia cepacia-catalysed hydrolyses of β-amino esters with H2O (0.5 equiv.) in t-BuOMe or in i-Pr2O at 45 °C are described. The enantiomers of biologically relevant β-arylalkyl-substituted β-amino acids, and especially (R)-3-amino-3-(2,4,5-trifluorophenyl)butanoic acid, the intermediate of the new antidiabetic drug sitagliptine, were prepared with high enantiomeric excesses (ee≥96%) and in good yields (≥42%). The Royal Society of Chemistry 2010.
Efficient synthesis of γ,δ-alkynyl-β-amino acid derivatives by a new copper-catalyzed amine-alkyne-alkyne addition reaction
Zhou, Lei,Jiang, Huan-Feng,Li, Chao-Jun
experimental part, p. 2226 - 2230 (2009/10/02)
A simple and efficient method for the synthesis of γ,δ-alkynyl- β-amino acid derivatives by a new copper-catalyzed amines-alkynes-alkynes addition was developed. Various γ,δ-alkynyl-β-amino acid derivatives were obtained in moderate to good yields in one step.