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By Y. Mastai

ISBN-10: 9535105817

ISBN-13: 9789535105817

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2000, 11, 809. ; Simon, H;. : Chirality 2001, 13, 29. : PhD disz. 2003 [25] a). ; Fogassy, E. b). Hung. Pat. no. ; Böcskei, Zs. Chirality, 1994, 6, 314 [27] Kassai, Cs: PhD diss. : Tetrahedron Letters, 1994, 35, 257260 . :. Tetrahedron: Asymmetry. 2008, 19, 1587. ; J. Pract. Chem. 1986, 336, 628. : J. Mol. Structure 1986, 147, 143. : Tetrahedron, 1985 41, 2841. :PhD theses. : Organic & Biomolecular Chemistry 2010 8, 347-359. J. J. Chem. , 1899, 75, 1066. C. Synthesis, 2003, 1626. : Tetrahedron: Asymmetry 2008,19, 519-536.

The obtained crystalline diastereoisomeric salt also will be a quasi-racemate, but its enantiomeric excess (ee: 93%) was even higher than that of the former case. It was also observed, that the average ee and F values of diastereoisomeric salts obtained at the resolutions (in number 28 resolutions) of racemic N-acetyl-phenylalanine and phenylglycine (AcPA and AcPG) with structurally similar bases (resolving agents) correspond to the eutectic composition (eeE value) of the adequate racemate (in these cases the enantiomers of the racemic compounds form racemates).

2006, 2599. [6] Ujj V; Schindler J; Novák T; Czugler M; Fogassy E; Keglevich Gy: Tetrahedron: Asymm. : Chem. , 2007, 3990-3996. : Chem. , 2007, 1071-1073. S. I. , 2007, 37, 55-60. : Organic & Biomolecular Chemistry 2010, 8, 347-359. ; Hirayama, N. ; Grofcsik, A. J. Chem. ; Reck, G. J. Chem. Soc. Perkin Trans. 2. C. Synthesis, 2003, 1626. ; Marthi, K. Chirality, 2007, 19, 239. [13] a). Hung. Pat. no. 214720, Chem. Abs. US Pat. 02133894 2001, Chem. Abs. 2001, 139, 90595 [14] a). , Leiserowitz L. Advances in Crystal Growth Research, Page: 381-400, 2001.

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