## Abstract Solvent‐induced chirality control in the enantioseparation of 1‐phenylethylamine **1** by __N__‐(__p__‐toluenesulfonyl)‐(__S__)‐phenylalanine **2** via diastereomeric salt formation was studied. **(S)‐1**·**(S)‐2** was preferentially crystallized as a less‐soluble salt from aqueous alco
Chiral discrimination in the energetics of formation of diastereomeric adducts involving polypeptides
✍ Scribed by G. Paradossi; B. Pispisa; R. Rizzo; M. Barteri
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1986
- Tongue
- English
- Weight
- 537 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Synopsis
Chiral discrimination in the energetics of formation of diastereomeric pairs between iron (IIIbcomplex ions bound to poly(L-glutamate) or poly (D-glutamate) and Lcatecholamines was measured by differential microcalorimetry at 25°C. When the association of substrates by Fe-polypeptide systems was virtually complete, diastereomeric discrimination energies of a few hundred calories per mol were observed, while diastereomeric discrimination entropies were found to be negligibly small. These results are consistent with the finding that the overall stereoselectivity in the electron transfer reaction between the optically active catecholamines and enantiomeric iron(II1) materials-corresponding to A(AG+) values around 900 cal/mol-is largely controlled by transition state effects in the kinetics.
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