## Abstract The ^1^H NMR 270‐MHz spectra of substituted 2‐phenylthiazolidines were recorded and the substituent‐induced chemical shifts (SCS) of the benzylic proton plotted against σ, the correlation coefficient being 0.801 and −ρ = 10.29 Hz. Halogens show deviations in the SCS plots. When the halo
1H NMR structural study of 2-phenylthiazolidine
✍ Scribed by A. Térol; G. Subra; J. P. Fernandez; Y. Robbe; J. P. Chapat; R. Granger
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 241 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Deuteration of 2‐phenylthiazolidine, and its complexation with the shift reagent tris(1,1,1,2,2,3,3‐heptafluoro‐7,7‐dimethyl‐4,6‐octanedionato)europium, have been used to study the signals and conformation of the heterocyclic protons and to interpret the ^1^H NMR spectrum of this 2‐substituted thiazolidine.
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