## Abstract The ^1^H CW off‐resonance decoupled ^13^C NMR spectra of pheromones and unsaturated fatty acids were measured for the determination of the configuration of double bonds of the type CH~2~CH CHCH~2~. The decoupling frequency corresponded to the resonance frequency of the CH~2~ proto
Benzazoles XIII—determination of the E and Z configuration of isomeric 2-(2-benzimidazolyl)-di- and -tetra-hydrothiophenes by IR, 1H and 13C NMR spectroscopy
✍ Scribed by P. Sohár; Gy. Mányai; K. Hideg; H. O. Hankovszky; L. Lex
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 335 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The configuration of the diastereomeric pairs of 2‐(3‐hydroxy‐3‐methyl‐5‐phenyl‐2,3‐dihydrothiophen‐2‐yl)benzimidazole (1a,1b) and 2‐(3‐hydroxy‐3‐methyltetrahydrothiophen‐2‐yl)benzimidazole (2a, 2b), as well as that of the acyl and diacyl derivatives of 2a and 2b, and the structure of the dehydrated products formed by heating 1a or 1b, and 2a or 2b, were determined by IR, ^1^H and ^13^C NMR spectroscopy.
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