## 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.
Unusual carbonyl carbon chemical shifts in the 13C nuclear magnetic resonance spectra of cyclic ketones
✍ Scribed by Peter Yates; Hillar Auksi; J. A. Gosbee; G. E. Langford; F. N. Maclachlan
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 217 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
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 comparisons with related compounds.
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