## Abstract The Ketonic ^13^C NMR signals of a series of 6‐hydroxy‐5‐oxobicyclo[2.2.2]oct‐7‐ene‐2‐carboxylic acid lactones and of haplophytine and related __N__‐substituted 3‐piperidinones occur at exceptionally high field; the structural factors which are responsible have been elucidated by compar
Carbon-13 nuclear magnetic resonance spectra of isomeric oxaziridines. Effects of the nitrogen lone pair on carbon-13 chemical shifts
✍ Scribed by Guy J. Jordan; DeLanson R. Crist
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 280 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The carbon‐13 n.m.r. spectra of several oxaziridines were measured. Aliphatic and aromatic ipso carbon atoms trans to the lone pair of nitrogen in oxaziridines were shifted upfield by c. 9 ppm, and 3.4 ppm, respectively, in comparison with isomers of inverted configuration. The results suggest that the nitrogen lone pair is partially responsible for the observed upfield shifts.
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## Abstract Carbon‐13 chemical shifts of the cyclopropyl carbons of eleven 4‐substituted cyclopropylbenzenes have been measured under conditions effectively corresponding to infinite dilution in DCCI~3~. The substituent‐induced chemical shifts (SCS) of __both__ the α and β carbons of the cyclopropa
## Abstract The ^13^C chemical shifts for 1,3‐dithiane and 9 methyl substituted derivatives are reported. Only three of the methyl‐1,3‐dithianes were conformationally anancomeric and hence the conformational equilibria must be taken into account when deriving the values of the different substituent