13C GIAO DFT calculation as a tool for configuration prediction of N-O group in saturated heterocyclic N-oxides

Copyright © 2012 John Wiley & Sons, Ltd.

Bibliographische Detailangaben
Veröffentlicht in:Magnetic resonance in chemistry : MRC. - 1985. - 50(2012), 6 vom: 04. Juni, Seite 415-23
1. Verfasser: Pohl, Radek (VerfasserIn)
Weitere Verfasser: Potmischil, Francisc, Dračínský, Martin, Vaněk, Václav, Slavětínská, Lenka, Buděšínský, Miloš
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Magnetic resonance in chemistry : MRC
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Carbon Isotopes Cyclic N-Oxides Piperidines Tropanes isopelletierine 4396-01-4 Cocaine I5Y540LHVR mehr... Nitrogen N762921K75 Oxygen S88TT14065
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520 |a Tropane, tropinone, pseudopelletierine and cocaine were oxidized in situ in a nuclear magnetic resonance (NMR) tube providing mixtures of exo/endo N-oxides. Observed (13)C chemical shifts were correlated with values calculated by gauge-including atomic orbitals density functional theory (DFT) OPBE/6-31G* method using DFT B3LYP/6-31G* optimized geometries. The same method of (13)C chemical shift calculation was applied on series of methyl-substituted 1-methylpiperidines and their epimeric N-oxides described in literature. The results show that using this undemanding calculation method enables assignment of configuration of N-O group in N-epimeric saturated heterocyclic N-oxides. The approach enables assigning of the configuration with high degree of certainty even if NMR data of only one isomer are available. An improved method of in situ oxidation of starting amines in an NMR tube is also described 
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650 4 |a Research Support, Non-U.S. Gov't 
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700 1 |a Potmischil, Francisc  |e verfasserin  |4 aut 
700 1 |a Dračínský, Martin  |e verfasserin  |4 aut 
700 1 |a Vaněk, Václav  |e verfasserin  |4 aut 
700 1 |a Slavětínská, Lenka  |e verfasserin  |4 aut 
700 1 |a Buděšínský, Miloš  |e verfasserin  |4 aut 
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