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12. Chiral HPLC study of compound 7a showed that the reaction between racemic mixture of amine 4b with racemic mixture of epoxide 15 gave 4 stereoisomers in equal amounts. Hence, the other reactions were assumed to give similar mixtures.
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14. All new compounds gave satisfactory microanalytical and spectral data. Optical rotations were measured in methanol, at 25°C for compounds 7b (+ 12.4°); 7c (-5.2°); 9a (-51.7°); 9b (-34.2°); 10a (-7.4°); 10b (+ 10.2°). Milnacipran 6 used to prepare compound 8 is a mixture of enantiomers.
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