## Abstract Well defined __E__/__Z__ isomers of __N__‐methoxy‐__p__‐nitrobenzimidoyl chloride, __N__‐methoxybenzimidoyl chloride, methyl __N__‐methylbenzohydroximate and ethyl __N__‐hydroxybenzimidate were prepared in order to provide model data for studies of benzhydroximic acid derivatives and re
E–Z isomerism of anilinomethylenemalonic acid derivatives
✍ Scribed by C. Bünz; D. Heber; U. Holzgrabe; U. Sürig
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 319 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The temperature and concentration dependence of the ^1^H NMR spectra of four anilinomethylenemalonic acid derivatives were determined in CDCl~3~ and DMSO‐d~6~ to assign the E–Z isomers and to investigate the formation of intra‐ and intermolecular hydrogen bonds. Chemical shifts and coupling constants in the ^13^C NMR spectra correspond with the results of the ^1^H NMR investigations in the case of the cyanoacetate ester derivative. Contradictory results for the acetoacetate derivative were found by semi‐empirical calculations.
📜 SIMILAR VOLUMES
1H and 15N NMR chemical shifts of 12 semicyclic amidinium salts are reported. Their E/Z equilibria in solution were analyzed by 1D and 2D 1H and 15N NMR techniques. In the solid state the Z-conÐguration is observed.
## Abstract 3′‐Epilutein (=(all‐__E__,3__R__,3′__S__,6′__R__)‐4′,5′‐didehydro‐5′,6′‐dihydro‐__β__,__β__‐carotene‐3,3′‐diol; **1**), isolated from the flowers of __Caltha palustris__, was submitted to both thermal isomerization and I~2~‐catalyzed photoisomerization. The structures of the main produc