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 |
Fingerprint
ASJC Scopus subject areas
- Chemistry(all)
- Materials Science(all)
Cite this
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. / Sohár, P.; Mányai, Gy; Hideg, K.; Hankovszky, H. O.; Lex, L.
In: Organic Magnetic Resonance, Vol. 14, No. 2, 1980, p. 125-128.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - 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
AU - Sohár, P.
AU - Mányai, Gy
AU - Hideg, K.
AU - Hankovszky, H. O.
AU - Lex, L.
PY - 1980
Y1 - 1980
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84986815929&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84986815929&partnerID=8YFLogxK
U2 - 10.1002/mrc.1270140209
DO - 10.1002/mrc.1270140209
M3 - Article
AN - SCOPUS:84986815929
VL - 14
SP - 125
EP - 128
JO - Magnetic Resonance in Chemistry
JF - Magnetic Resonance in Chemistry
SN - 0749-1581
IS - 2
ER -