Abstract
A series of tri- and tetrasubstituted 4-piperidones and their bicyclic analogs has been synthesized. It was established by 1H NMR spectroscopy that all the piperidones obtained have the chair conformation in solution with equatorially disposed substituents.
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Vatsadze, S.Z., Krainova, Y.V., Kovalkina, M.A. et al. Synthesis of Polysubstituted 1,4-Diazacycloheptan-5-ones. 1. Synthesis and Conformational Investigation of Polysubstituted 4-Piperidones. Chemistry of Heterocyclic Compounds 36, 1185–1191 (2000). https://doi.org/10.1023/A:1002820816850
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DOI: https://doi.org/10.1023/A:1002820816850