@article{209,
  author = {Miklós F. and István Mándity and Sillanpää R. and Fülöp F.},
  title = {Stereocontrolled synthesis of five diastereomers of trimethyl 3-aminocyclopentane-1,2,4-tricarboxylates},
  abstract = {The sterically controlled oxidative cleavage of N-protected diexo- and diendo-substituted norbornene β-amino acids/esters resulted in four trimethyl 3-aminocyclopentane-1,2,4-carboxylate diastereomers. The sodium methoxide mediated isomerization of the four diastereomers in all cases yielded the thermodynamically most stable all-trans stereoisomer as a single product. © 2013 Elsevier Ltd. All rights reserved.},
  year = {2013},
  journal = {Tetrahedron Letters},
  volume = {54},
  number = {29},
  pages = {3769–3772},
  address = {Ma, D., Ma, J., Dai, L., (1997) Tetrahedron: Asymmetry, 8, pp. 825-827;},
  issn = {0040-4039},
}