## Abstract The analysis of the ^13^C NMR chemical shifts of 16 substituted 2‐phenylthiazolidines shows that the 1,3‐thiazolid‐2‐yl group exerts a deshielding effect at the __ipso__ carbon (C‐1′) and shielding effects at the __ortho__ and __para__ positions of the benzene ring (C‐2′ and C‐4′), and
An NMR study of 2-alkoxy-1,3,2-dioxaphospholanes. I—13C chemical shifts
✍ Scribed by D. Besserre; S. Coffi-Nketsia
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 410 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Measurements of the ^13^C chemical shifts of 2‐alkoxy‐1,3,2‐dioxaphospholanes have allowed the determination of the contribution of the substituent to the α‐, β‐ and γ‐carbon chemical shifts of attached alkyl groups. The preliminary assignments of the signals were made using the following information; relative intensities, variations in coupling constants J(^31^P^13^C) and the existence of linear correlations between the shifts of carbon atoms in the P‐alkoxy groups and the degree of substitution of the observed carbon or of its neighbours.
📜 SIMILAR VOLUMES
Complete 13C NMR chemical shift assignments are reported for 32 cyclic and one acyclic 1.3-diketones, either unsubstituted or having one or two substituents at the 2-position. The first two classes exist exclusively in the enol form in (CD,),SO and as mixed tautomers in CDCI,.
## Abstract The ^13^C NMR spectra of 26 substituted 2‐azabicyclo[3.3.1]nonan‐7‐ones are reported, providing a diagnostic method for the stereochemical elucidation of the relative configuration of these products.
## Abstract The ^13^C NMR spectra of a series of 2‐X‐4‐Y‐5‐Z‐substituted 2H‐pyridazin‐3‐ones were measured and assigned on the basis of results from one‐dimensional semi‐selective INEPT or one‐dimensional relayed coherence transfer (HICUUP) experiments.