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Levrat, F., Stoeckli-Evans, H. and Engel, N. (2002) Enantiomeric excess determination of α-amino acids by 19F NMR spectroscopy of their N,N-dimethyl-(2,2,2- trifluoro-1-phenylethyl)amine-C,N)palladium complexes. Tetrahedron: Asymmetry, 13, 2335-2344.

has been cited by the following article:

• TITLE: Chiral palladium complexes based on derivatives of benzylamine and 2α-hydroxypinan-3-one

  AUTHORS: Olga A. Zalevskaya, Yana A. Gur'eva, Larisa L. Frolova, Igor N. Alekseev, Alexander V. Kutchin

  KEYWORDS: Palladium Complexes; Cyclopalladation; Chiral Imine; Amine

  JOURNAL NAME: Natural Science, Vol.2 No.11, November 30, 2010

  ABSTRACT: Synthesized and characterized new chiral palladium complexes, some of which contain asymmetric donor nitrogen atom. Nitrogen-containing derivatives (+) - and (-)-2α-hydroxypinan-3-one- (1R,2R,5R)-3-(benzylimino)-2,6,6-trimethylbicy- clo[3.1.1]heptane-2-ol (HL1), (1S,2S,3S,5S)-3- (benzylamino)-2,6, 6-trimethylbicyclo[3.1.1]- heptane-2-ol (HL2), (1R,2R,5R)-3-((S)-α-methyl- benzylimino)-2,6,6-trimethylbicyclo[3.1.1]- heptane-2-ol (HL3), (1R,2R,3R,5R)-3-((S)-α-methyl- benzylamino)-2,6,6-trimethylbicyclo[3.1.1]- heptane-2-ol (HL4) -were studied as optically active ligands.