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The enantiomeric purity of the products was determined by glc using a Bondex β stationary phase: Fischer, P.; Aichholz, R.; Bölz, U.; Juzu, M.; Krimmer, S. Angew. Chem. 1990, 102, 439; Angew. Chem. Intl. Ed. Engl. 1990, 29, 427. Since in a kinetic resolution the enantiomeric excess of product and starting material varies as the reaction proceeds, it is more meaningful to use the E-value (enantiomeric ratio; measures the ability of the enzyme to distinguish between enantiomers) to compare reactions (see ref. 1, cit, ref.). A simple program to calculate the E-value for given enantiomeric ratios is available free of charge at http://www-orgc.tu-graz.ac.at: Kroutil, W.; Kleewein, A.; Faber, K. Tetrahedron: Asymmetry 1997, 8, 3251.
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Alternative synthesis of (3-phenylcyclopropyl)methanol (93% ee) using equimolar amounts of a chiral modifier: Charette, A. B.; Lebel, H. Org. Synth. 1998, 76, 86.
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41
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84920346883
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note
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12O (148.20): calcd. C 81.04, H 8.16; found C 81.03, H 8.21.
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