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A few intramolecular examples of amine-catalyzed aza-Michael reactions have also appeared: Fustero, S.; Moscardó, J.; Jiménez, D.; Pérez-Carrión, M. D.; Sánchez-Roselló, M.; del Pozo, C. Chem.-Eur. J. 2008, 14, 9868
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All aza-Michael products were found to be configurationally unstable, undergoing fast racemization upon standing at rt
-
All aza-Michael products were found to be configurationally unstable, undergoing fast racemization upon standing at rt.
-
-
-
-
34
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78651473920
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In all cases in which the S -adduct 5a was isolated, it was obtained as a racemic mixture
-
In all cases in which the S -adduct 5a was isolated, it was obtained as a racemic mixture.
-
-
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35
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78651520322
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CCDC 782265 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
CCDC 782265 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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