262858-33-3Relevant academic research and scientific papers
Fast ester cleavage of sterically hindered α- and β-aminoesters under non-aqueous conditions. Application to the kinetic resolution of aziridine esters
Alezra, Valérie,Bouchet, Céline,Micouin, Laurent,Bonin, Martine,Husson, Henri-Philippe
, p. 655 - 658 (2000)
Various protected α- and β-aminoesters undergo fast ester cleavage by treatment with t-BuOK in THF. The accelerating effect of a neighboring chelating group was used for the efficient kinetic resolution of non-racemic aziridine esters. (C) 2000 elsevier Science Ltd.
The Dakin-West reaction of N-alkoxycarbonyl-N-alkyl-α-amino acids employing trifluoroacetic anhydride
Kawase, Masami,Hirabayashi, Michitaka,Kumakura, Hiroko,Saito, Setsuo,Yamamoto, Katsumi
, p. 114 - 119 (2007/10/03)
The Dakin-West reaction of N-alkoxycarbonyl-N-alkyl-α-amino acids (1a - j) with trifluoroacetic anhydride in the presence of pyridine gave α-amido trifluoromethyl ketones (2a - j), in which probable intermediates were mesoionic 1,3-oxazolium-5-olates (munchnones). The diastereoselective reduction of 2a - f with NaBH4 gave the threo-aminoalcohols (5a - f), which may be explained by the Felkin-Anh model. This was confirmed by converting 5a - f into trans-5-trifluoromethyl-2-oxazolidinones (6a - f) in good yields.
