Configurational and conformational studies of N,N-dimethylpiperidinium derivatives by 13C and 1H NMR spectroscopy
β Scribed by A. F. Casy; F. O. Ogungbamila
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 449 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Abstract
The ^13^C and ^1^H NMR spectra of a series of methiodides of monoβ and diβCβmethyl derivatives of 1βmethylβ4βphenylβ4βpiperidinols are reported and chemical shift data analysed in terms of configurations and conformations of isomeric sets. Results demondtrate the value of quaternary salt NMR data as an aid to configurational assignment, and the evaluation of nonβbonded interactions governing conformational equilibria in piperidine derivatives.
π SIMILAR VOLUMES
## Abstract The ^13^C chemical shift of the substituted or functionalized carbon of various medium and large rings is plotted against ring size (6β15 carbons). The curves thus obtained allow a conformational analysis of the corresponding derivatives.
Pyridofuroxan ([1,2,5]oxodiazolo [3,4-b]pyridine 1-oxide) undergoes isomerization between the N1oxide and N3-oxide forms which can be observed by the 1 H, 13 C and 15 N NMR spectroscopy but not by 14 N and 17 O NMR at ambient and low temperatures. The rearrangement becomes slower at low temperatures
The "C and 'H NMR spectra of six N-5'-methylsalicylideneanilines have been studied. Correlations of the chemical shifts of C-a (azomethine carbon) and C-4' with the cr, F, R , crI and a: parameters have been examined for N-5'-methylsalicylideneanilines, and also for N-benzylideneanilines and N-salic