## Abstract The ^13^C^13^C spin–spin coupling constants in natural abundance oxetane, thietane, cyclobutanone, bromo‐and chlorocyclobutane have been measured. Furthermore, the ^13^C isotope‐induced changes in the chemical shifts of the different ^13^C nuclei in the molecules mentioned above are re
13C chemical shifts and 13C13C coupling constants of some alkyl(aryl)sulphonates
✍ Scribed by C. Millot; J. Brondeau; D. Canet
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 237 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The attachment of an ester group at C-4 (1) and lactone bridges between C-6 and C-8 (1); C-2 and C-4, C-6 and C-8 (2); C-4 and C-6 (4) resulted in C-4, C-5 and C-6 showing similar chemical shifts in all three structures. In Diosbulbins A (1) and B (Z), C-12 bearing the equatorial furan ring is in an R configuration: while the configuration of the same carbon in Diosbulbins D (3) and G (4) is the opposite.6
During this investigation it was found that the APT was very sensitive to J values. This, therefore, required several experiments to be performed to obtain the correct results. The DEPT rneth~d,'~ which could have overcome these difficulties, was not availble to us at the time of this investigation.
📜 SIMILAR VOLUMES
## Abstract Long range inter‐ring ^13^C^13^C couplings are found to be effective in the title compounds, and the magnitudes of coupling constants and of substituent effects on ^13^C chemical shifts, as well as the signs of the latter, alternate with respect to the number of connecting bonds.
## Abstract The effects of an hydroxy substituent on ^13^C^13^C coupling constants and ^13^C chemical shifts have been measured in 1‐hydroxynaphthalene‐2‐^13^C and 1‐hydroxypyrene‐1‐^13^C. The changes observed in the ^13^C^13^C couplings show the effect of a substituent attached directly to the l
## Abstract Measurement of the ^13^C NMR spectra of the bridgehead nitro compounds __1a–5a__ has been performed. It is found that one‐bond ^13^C^15^N coupling is not necessarily a reflection of the degree of s character of the bridgehead carbon exocyclic bonding orbital. Although the magnitude of
## Abstract One bond ^13^C,^13^C‐ and ^13^C,^1^H‐coupling constants have been measured for some 1,2‐dimethylene‐cycloalkanes, as well as for 2,3‐dimethylbuta‐1,3‐diene and methylenecyclobutane. The results for 2,3‐dimethylbuta‐1,3‐diene confirm the findings for buta‐1,3‐diene, i.e. that __J__(C‐1,