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The results with (Rp,R)-7 are in contradiction to findings reported by S. Bräse, St. Dahmen, S. Höfener, F. Lauterwasser, M. Kreis, R. E. Tiegert, Synlett 2004, 2647-2669 in a review article. Whereas in our hands iminophenol (Rp,R)-7 leads to S-configured 1-phenylpropanol (with 16% ee, and the diastereomer (Rp,S)-7 provides the S-configuration also (at 55% ee, Bräse and co-workers report that it is the (Sp,S)-stereoisomer that provides the S-configuration (20% ee, whereas the (Rp,S)-diastereomer leads to the R-configuration (59% ee) of the alcohol. Unfortunately the original samples to resolve this contradiction are no longer available
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The results with (Rp,R)-7 are in contradiction to findings reported by S. Bräse, St. Dahmen, S. Höfener, F. Lauterwasser, M. Kreis, R. E. Tiegert, Synlett 2004, 2647-2669 in a review article. Whereas in our hands iminophenol (Rp,R)-7 leads to S-configured 1-phenylpropanol (with 16% ee), and the diastereomer (Rp,S)-7 provides the S-configuration also (at 55% ee), Bräse and co-workers report that it is the (Sp,S)-stereoisomer that provides the S-configuration (20% ee), whereas the (Rp,S)-diastereomer leads to the R-configuration (59% ee) of the alcohol. Unfortunately the original samples to resolve this contradiction are no longer available.
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