Study of the mechanism of optical resolutions via diastereoisomeric salt formation

[1]  E. Fogassy,et al.  Physico-chemical investigation of the diastereoisomeric salt pair formed by α-phenyl-ethyl-amine and R-1-phenylethyl-succinamic acid , 1995 .

[2]  S. Larsen,et al.  The role of solvates in optical resolution. A study of the diastereoisomeric salts formed from enantiomeric 2-amino-2-phenylethanol and (R)-mandelic acid, their crystal structures and physico-chemical properties , 1994 .

[3]  M. Ács,et al.  Study of the mechanism of the optical resolution of N-methylamphetamine via diastereoisomeric salt formation by the Pope-Peachey method , 1994 .

[4]  E. Fogassy,et al.  Predictions of which diastereoisomeric salt precipitates during an optical resolution via diastereoisomeric salt formation , 1994 .

[5]  S. Larsen,et al.  Optical Resolution Through Diastereomeric Salt Formation: the Crystal Structures of Cinchoninium (R)-Mandelate and Cinchoninium (S)-Mandelate at Low Temperature , 1993 .

[6]  G. Pokol,et al.  Calculation of the efficiency of optical resolutions on the basis of the binary phase diagram for the diastereoisomeric salts , 1992 .

[7]  E. Novotny-Bregger,et al.  Structural aspects of optical resolutions. Optical resolution of (R,S)-mandelic acid. DSC and X-ray studies of the diastereoisomeric salts , 1992 .

[8]  A. McPhail,et al.  Chiral discrimination in the structures and energetics of association of stereoisomeric salts of mandelic acid with .alpha.-phenethylamine, ephedrine, and pseudoephedrine , 1988 .

[9]  M. Czugler,et al.  Structural studies on optical resolution via diasteroisomeric salt formation. Enantiomer separation for cis-permethrinic acid [cis-2,2-dimethyl-3- (2,2-dichlorovinyl)cyclopropanecarboxylic acid] , 1988 .

[10]  P. Taylor,et al.  Asymmetric resolution and molecular recognition. Part 2. The X-ray crystal structures of ephedrine–N-benzyloxycarbonyl-L-leucine and ephedrine–N-acetyl-L-valine , 1986 .

[11]  G. Snatzke.  J. Jaques, A. Collet, and S. H. Wilen: Enantiomers, Racemates, and Resolutions, J. Wiley & Sons, Inc., New York, Chichester, Brisbane, Toronto 1981. 447 Seiten, Preis: £ 38.75 , 1982 .

[12]  Jean Jacques,et al.  Enantiomers, Racemates, and Resolutions , 1981 .

[13]  E. Fogassy,et al.  PREPARATION OF L- AND D-1-( 4'-BROMPHENYL)-2- METHYL-AMINO-PROPANE AND STUDY OF ITS CONFIGURATION , 1978 .

[14]  J. Jacques,et al.  Strategies in optical resolutions , 1977 .

[15]  Y. Shimura,et al.  Optical Resolution and Ternary System Solubility Isotherms of Cobalt(III) Complex Salts , 1977 .

[16]  M. Leclercq,et al.  Détermination de la pureté optique d'un corps cristallin par calorimétrie—II , 1970 .

[17]  G. Miana,et al.  A new general method for the regeneration of optically active acids and bases from resolved salts , 1967 .

[18]  J. Jacques,et al.  Determination de la purete optique d'un corps cristallin par une methode calorimetrique , 1967 .

[19]  H. Dakin.  THE RESOLUTION OF INACTIVE MALIC ACID INTO OPTICALLY ACTIVE FORMS , 1924 .