Beilstein J. Org. Chem. 2018, 14, 553–559.
14.Held, F. E.; Tsogoeva, S. B. Catal. Sci. Technol. 2016, 6, 645–667.
the desired Michael adduct 7 was obtained in 75% yield as a
mixture of diastereomers (dr 68:32) with very high enan-
tiomeric purity of the major diastereomer (er 99:1). With the
help of quantum-chemical calculations, we have proposed a
transition state model for the Michael addition.
15.Bassas, O.; Huuskonen, J.; Rissanen, K.; Koskinen, A. M. P.
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Supporting Information
18.Baran, R.; Veverková, E.; Škvorcová, A.; Šebesta, R.
19.Veverková, E.; Bilka, S.; Baran, R.; Šebesta, R. Synthesis 2016, 48,
Supporting Information File 1
Experimental procedures, characterization data for all
compounds, pictures of NMR spectra and computational
details.
20.Bae, H. Y.; Song, C. E. ACS Catal. 2015, 5, 3613–3619.
21.Sim, J. H.; Song, C. E. Angew. Chem., Int. Ed. 2017, 56, 1835–1839.
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24.Porta, R.; Benaglia, M.; Coccia, F.; Rossi, S.; Puglisi, A. Symmetry
Acknowledgements
This publication is the result of the project implementation:
26240120025 supported by the R&DOP funded by the Euro-
pean Regional Development Fund.
25.Martinez, C. A.; Hu, S.; Dumond, Y.; Tao, J.; Kelleher, P.; Tully, L.
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