## Abstract The configurations and conformations of diastereoisomeric 1‐(decahydroquinolin‐8‐yl)butan‐2‐ols and of perhydropyrido[3,2,1‐__j,k__][3,1]benzoxazepines resulting from ring closure of these compounds with formaldehyde have been assigned by ^1^H and ^13^C NMR spectroscopy.
Compounds with bridgehead nitrogen 68—NMR spectra and stereochemistry of perhydropyrido [1,2-c] [1,3]oxazines
✍ Scribed by Trevor A. Crabb; Simon T. Ingate; Thomas G. Nevell
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 238 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Low‐temperature ^13^C NMR spectroscopy shows perhydropyrido [1,2‐c] [1,3]oxazine to adopt a conformational equilibrium in CD~2~Cl~2~–CFCl~3~ solution containing 98% trans fused conformer in equilibrium with 2% O‐outside‐cis fused conformer at 203 K. A similar equilibrium position is adopted by the trans‐(H‐4,H‐4a)‐4‐methylperhydropyrido[1,2‐c][1,3]oxazine, whereas the C‐4 epimer adopts exclusively the trans fused conformation.
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