Rationalization and prediction of solution enantiomeric excess in ternary phase systems.

[1]  C. Ching,et al.  Investigation of the phase diagrams of chiral praziquantel. , 2006, Chirality.

[2]  M. Mazzotti,et al.  Solid-Liquid Equilibrium of Troger's Base Enantiomers in Ethanol: Experiments and Modelling , 2004 .

[3]  H. Morowitz A mechanism ffr the amplification of fluctuations in racemic mixtures. , 1969, Journal of theoretical biology.

[4]  Kenso Soai,et al.  Asymmetric autocatalysis and amplification of enantiomeric excess of a chiral molecule , 1995, Nature.

[5]  V. Maddaiah A model for hormone specific activation of adenyl cyclase. , 1969, Journal of theoretical biology.

[6]  A. Seidel-Morgenstern,et al.  Enantiomeric mandelic acid system-melting point phase diagram and solubility in water , 2002 .

[7]  J. Amend,et al.  Solubilities of the common L-α-amino acids as a function of temperature and solution pH , 1997 .

[8]  Ernest L. Eliel,et al.  Stereochemistry of Organic Compounds , 1962 .

[9]  D. Hashizume,et al.  Large nonlinear effect observed in the enantiomeric excess of proline in solution and that in the solid state. , 2006, Angewandte Chemie.

[10]  F. Frank,et al.  On spontaneous asymmetric synthesis. , 1953, Biochimica et biophysica acta.

[11]  Lian Yu,et al.  Effect of Molecular Chirality on Racemate Stability: α-Amino Acids with Nonpolar R Groups , 2006 .

[12]  Physicochemical properties, binary and ternary phase diagrams of ketoprofen. , 2004 .

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

[14]  Hiroshi Iwamura,et al.  Thermodynamic control of asymmetric amplification in amino acid catalysis , 2006, Nature.

[15]  Stephen Suresh,et al.  dl‐Proline Monohydrate , 1995 .