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, 1H and 13C NMR spectroscopy.
| Original language | English |
|---|---|
| Pages (from-to) | 125-128 |
| Number of pages | 4 |
| Journal | Organic Magnetic Resonance |
| Volume | 14 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 1980 |
ASJC Scopus subject areas
- Chemistry(all)
- Materials Science(all)
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Cite this
Sohár, P., Mányai, G., Hideg, K., Hankovszky, H. O., & Lex, L. (1980). 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. Organic Magnetic Resonance, 14(2), 125-128. https://doi.org/10.1002/mrc.1270140209