## Abstract The configuration and conformation of __Z__‐ and __E__‐__N__‐methyl‐ and ‐__N__‐benzyl‐2‐__p__‐nitrophenyl‐4,5‐, and ‐5,6‐tetramethylenetetrahydro‐1,3‐oxazines were determined by ^1^H and ^13^C NMR spectroscopy. The __Z__ isomers were proved to be conformationally homogeneous, having th
Configurations and conformations of cis- and trans-N-methyl- and -N-benzyl-4,5- and -5,6-tetramethylenetetrahydro-1,3-oxazines
✍ Scribed by P. Sohár; F. Fülöp; G. Bernáth
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 384 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The con6gurations and conformations of cis-and tram-N-methyl-and -N-benzyl-4,5-and -5,6tetramethylenetetrahydm-l,3-o~es were determined by 'H and -C NMR spectroscopy. The cis isomers are conformationally homogeneous, having the hetero atom attached to the cydohexyl ring, in the axial and equatorial positions, respectively, in the 5,6and 45-tetramethylene compounds, similar to the case of the 2-p-nitrophenyl-substituted analogues investigated previously.
📜 SIMILAR VOLUMES
The N-methyl and N,N-dimethyl derivatives of cisand rruns-2-( 3,4,5-trimethoxyphenyl)cyclohexylamines were prepared for evaluation of psychotropic activity. Synthesis by catalytic reductive methylation and characterization by NMR spectroscopy are reported. Magnetic nonequivalence of the methyl group
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