Analysis of the 'H NMR spectra of several monothiocsrbonohydraones, some of them synthesized for the first time, shows that they exist as two structural isomers. Whereas, in general, the derivatives of aromatic aldehydes conform to a linear structure, the aliphatic carbonyl derivatives conform to he
Structural assignment of isomeric chain demethylated retinals by 1H NMR spectroscopy
โ Scribed by A. D. Broek; J. M. L. Courtin; J. R. Mellema; J. Lugtenburg; K. Nicolay; K. Dijkstra; R. Kaptein
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 234 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
Abstract
Geometric isomers of allโtransโ9โdemethylโ, โ13โdemethylโ and โ9,13โbisdemethylretinal were prepared. The 360 MHz ^1^H NMR spectra of 13 geometric isomers of these three demethylated retinal systems have been measured. The chemical shift and coupling constant values in each case allowed an unambiguous assignment of the structure of each compound.
๐ SIMILAR VOLUMES
## Abstract The stereochemistry of various pairs of isomeric 2โcyclohexenโ1โylidenecyanoacetates was assigned using ^1^H NMR spectroscopy. The isomers with the ฮณโmethylene or the ฮณโvinyl protons __cis__ to the carbalkoxy group were found to have the signals of these protons at approximately 0.3 ppm
The structural assignment of 2-and 4-endo-iodobicydo[3.3.l]non-6-ene-3-endo-~bonitriles was accomplished by evaluation of their COSY spectra. All 'H and =C signals were identified unequivocally. Vicioal 'H-lH coupling constants, NOESY experiments and iodine substitnent effects on the -C chemical shi