## Abstract ^1^H NMR of the tricyclic molecule 3 โ Cyano โ1,2,2โ trimethyl โ 6 โ azatricyclo โ[3.3.1.0^3,8^]nonโ6โene does not permit the distinction between this structure and the other regioisomer that can be formed in a photochemically induced reaction. The elucidation of the structure was possi
Structural assignment of the isomeric 2- and 4-endo- iodobicyclo[3.3.1]non-6-ene-3-endo- carbonitriles by two-dimensional 1H and 13C NMR spectroscopy
โ Scribed by Helmut Duddeck; Manfred Kaiser; Dino Brosch
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 443 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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โฆ Synopsis
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 shifts show that these molecules prefer the chair conformation.
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The total assignment of the 13C and the ' H NMR spectra of four derivatives of 1,3diaza-2,4-diboranaphthalene has been performed. The interpretation of the spectra was achieved from the concerted application of direct and long-range heteronuclear chemical shift correlation and homonuclear COSY two-d
## Abstract The ^1^H NMR spectrum of naphtho [1โฒ,2โฒ:4,5]thieno[2,3โ__c__]quinoline is highly congested because all the protons are in an aromatic environment, and the structure of the molecule is nearly symmetric. With this in mind, the assignment of the ^1^H and ^13^C NMR spectra of this compound
## Abstract The 1,3โdipolar addition reaction of acrylonitrile to the betaine 1โphenyl or methylโ3โoxidopyridinium is not so highly regioselective as generally assumed. New regioisomers are isolated. Their structures are proven by mass spectroscopy and protonโand carbonโNMR spectroscopy. Some 3,4di
The 1H and 13C NMR spectra of cis-endo (a) and cis-exo (b) diastereoisomeric pairs of รve di โ erently C-1-functionalized 2,4-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-ones were completely assigned. Several trends regarding the variation of chemical shifts and coupling constants of hydrogen and carbon a