## Abstract ^13^C NMR Substituent chemical shift (SCS) increments have been determined for the carbonyl carbon of a variety of substituted benzaldehydes and acetophenones. The ^13^C NMR chemical shift of the carbonyl carbon can be predicted for many di‐ and trisubstituted benzaldehydes and acetophe
C-13 chemical shifts of the carbonyl group—VI: Transannular interactions in mesocyclic compounds
✍ Scribed by Thomas T. Nakashima; Gary E. Maciel
- Publisher
- John Wiley and Sons
- Year
- 1972
- Tongue
- English
- Weight
- 350 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
The utility of C-13 NMR in detecting transannular interactions of a carbonyl group with 4-, -S-and -N-in eight-membered ring compounds has been studied. The C-13 carbonyl chemical shifts were determined in two solvents, employing frequency-sweep and pulse/Fourier transform techniques. The results confirm earlier conclusions based upon other physical methods and indicate that C-13 NMR should prove useful in studies of such interactions.
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