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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 29, 1999 - Issue 24
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Original Articles

Optical Resolution in two Immiscible Solvents in the Presence of an Intermediate Solvent. Optical Resolution of N-Methyl-Amphetamine by O,O′-Dibenzoyl-R,R-Tartaric Acid in Dichloroethane-Water-Methanol Solvent System

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Pages 4315-4319 | Published online: 25 Sep 2007

References

  • Newman, P., 1978–84. Optical Resolution Procedures for Chemical Compounds. Vol. vols.1–3. New York: Optical Resolution Information Center, Manhattan College; 1978–84.
  • Sheldon, R. A., 1993. Chirotechnology. New York: Marcel Dekker Inc.; 1993.
  • Jacques, J., Collet, A., and Wilen, S. H., 1981. Enantiomers, Racemates and Resolutions. New York: Wiley and Sons; 1981. p. 383.
  • Ács, M., Fogassy, E., and Faigl, F., 1985. Tetrahedron 41 (1985), p. 2465.
  • Fogassy, E., Ács, M., Faigl, F., Simon, K., Rohonczy, J., and Ecsery, Z., 1986. J. Chem. Soc. Perkin Trans. 2 (1986), p. 1881.
  • Kozma, D., Madarász, Z., Ács, M, and Fogassy, E., 1994. Tetrahedron Asymmetry 5 (1994), p. 193.
  • Fogassy, E., Lopata, A., Faigl, F., Darvas, F., Ács, M., and Töke, L., 1980. Tetrahedron Lett. 21 (1980), p. 647, The efficiency (0<S<1) of the optical resolution has been defined as the product of the optical purity (0<OP<1) and the yield (0<Y<1) of the precipitated salt: S= OP×Y, in.
  • Kozma, D., and Fogassy, E., 1997. Enantiomer 2 (1997), p. 51.

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