Synthesis and conformational properties of substituted 1,4,2-oxazasilinanes low temperature NMR study and quantum chemical calculations
- A number of N-substituted 2,2-dimethyl-1,4,2-oxazasilinanes 1 were synthesized and studied by variable temperature dynamic H-1 and C-13 NMR spectroscopy, room temperature N-15 NMR spectroscopy and theoretical calculations at the DFT and MP2 levels of theory. Both the preferred conformers were assigned and the barrier to the ring inversion of the saturated six-membered ring determined. From 1 the corresponding methyl iodide salts were produced, their structure studied by X-ray analysis and found to be in excellent agreement with the results of the theoretical calculations.
Verfasserangaben: | Nataliya F. Lazareva, Alexander I. Albanov, Bagrat A. Shainyan, Erich KleinpeterORCiDGND |
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DOI: | https://doi.org/10.1016/j.tet.2011.11.077 |
ISSN: | 0040-4020 |
Titel des übergeordneten Werks (Englisch): | Tetrahedron |
Verlag: | Elsevier |
Verlagsort: | Oxford |
Publikationstyp: | Wissenschaftlicher Artikel |
Sprache: | Englisch |
Jahr der Erstveröffentlichung: | 2012 |
Erscheinungsjahr: | 2012 |
Datum der Freischaltung: | 26.03.2017 |
Freies Schlagwort / Tag: | 1,4,2-Oxazasilinanes; Conformational analysis; Dynamic NMR; Quantum chemical calculations; X-ray analysis |
Band: | 68 |
Ausgabe: | 4 |
Seitenanzahl: | 8 |
Erste Seite: | 1097 |
Letzte Seite: | 1104 |
Fördernde Institution: | Russian Foundation for Basic Research; Deutsche Forschungsgemeinschaft [11-03-91334] |
Organisationseinheiten: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie |
Peer Review: | Referiert |